http://fasb.org/us-gaap/2025#PrepaidExpenseAndOtherAssetsCurrenthttp://fasb.org/us-gaap/2025#OtherNonoperatingIncomeExpensehttp://fasb.org/us-gaap/2025#OtherNonoperatingIncomeExpensehttp://fasb.org/us-gaap/2025#OtherNonoperatingIncomeExpensehttp://www.merit.com/20250630#BusinessCombinationContingentConsiderationArrangementsContingentConsiderationBenefithttp://www.merit.com/20250630#BusinessCombinationContingentConsiderationArrangementsContingentConsiderationBenefithttp://www.merit.com/20250630#BusinessCombinationContingentConsiderationArrangementsContingentConsiderationBenefit0000856982--12-312025Q2falseMERIT MEDICAL SYSTEMS INC5921800058743000http://fasb.org/us-gaap/2025#PrepaidExpenseAndOtherAssetsCurrentP5DP10DP10DP20DP30DP20DP30Dhttp://fasb.org/us-gaap/2025#SecuredOvernightFinancingRateSofrMemberhttp://fasb.org/us-gaap/2025#OtherNonoperatingIncomeExpensehttp://www.merit.com/20250630#BusinessCombinationContingentConsiderationArrangementsContingentConsiderationBenefit25670000000856982us-gaap:CommonStockMember2025-04-012025-06-300000856982us-gaap:CommonStockMember2024-04-012024-06-300000856982us-gaap:RetainedEarningsMember2025-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2025-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2025-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-06-300000856982us-gaap:RetainedEarningsMember2025-03-310000856982us-gaap:AccumulatedTranslationAdjustmentMember2025-03-310000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2025-03-310000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-03-310000856982us-gaap:RetainedEarningsMember2024-12-310000856982us-gaap:AccumulatedTranslationAdjustmentMember2024-12-310000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-12-310000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-12-310000856982us-gaap:RetainedEarningsMember2024-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2024-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-06-300000856982us-gaap:RetainedEarningsMember2024-03-310000856982us-gaap:AccumulatedTranslationAdjustmentMember2024-03-310000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-03-310000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-03-310000856982us-gaap:RetainedEarningsMember2023-12-310000856982us-gaap:AccumulatedTranslationAdjustmentMember2023-12-310000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2023-12-310000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2023-12-310000856982us-gaap:EmployeeStockOptionMember2024-01-012024-06-300000856982srt:MaximumMemberus-gaap:PerformanceSharesMember2025-01-012025-06-300000856982srt:MaximumMemberus-gaap:PerformanceSharesMember2024-01-012024-06-300000856982us-gaap:PerformanceSharesMember2024-01-012024-06-300000856982us-gaap:RestrictedStockUnitsRSUMember2024-01-012024-06-300000856982mmsi:CashSettledPerformanceSharesMember2024-12-310000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:ShareBasedPaymentArrangementNonemployeeMember2025-01-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:ShareBasedPaymentArrangementEmployeeMember2025-01-012025-06-300000856982mmsi:EndoGastricSolutionsIncMember2025-01-012025-06-300000856982mmsi:CookMedicalHoldingsLlcMember2025-01-012025-06-300000856982mmsi:PeripheralInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:PeripheralInterventionMembercountry:USmmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:OEMMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:OEMMembercountry:USmmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:EndoscopyDevicesMemberus-gaap:NonUsMembermmsi:EndoscopySegmentMember2025-04-012025-06-300000856982mmsi:EndoscopyDevicesMembercountry:USmmsi:EndoscopySegmentMember2025-04-012025-06-300000856982mmsi:CustomProceduralSolutionsMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:CustomProceduralSolutionsMembercountry:USmmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:CardiacInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:CardiacInterventionMembercountry:USmmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982us-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:PeripheralInterventionMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:OEMMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:EndoscopyDevicesMembermmsi:EndoscopySegmentMember2025-04-012025-06-300000856982mmsi:CustomProceduralSolutionsMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:CardiacInterventionMembermmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982country:USmmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982us-gaap:NonUsMember2025-04-012025-06-300000856982country:US2025-04-012025-06-300000856982mmsi:PeripheralInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:PeripheralInterventionMembercountry:USmmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:OEMMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:OEMMembercountry:USmmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:EndoscopyDevicesMemberus-gaap:NonUsMembermmsi:EndoscopySegmentMember2025-01-012025-06-300000856982mmsi:EndoscopyDevicesMembercountry:USmmsi:EndoscopySegmentMember2025-01-012025-06-300000856982mmsi:CustomProceduralSolutionsMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:CustomProceduralSolutionsMembercountry:USmmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:CardiacInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:CardiacInterventionMembercountry:USmmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982us-gaap:NonUsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:PeripheralInterventionMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:OEMMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:EndoscopyDevicesMembermmsi:EndoscopySegmentMember2025-01-012025-06-300000856982mmsi:CustomProceduralSolutionsMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:CardiacInterventionMembermmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982country:USmmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982us-gaap:NonUsMember2025-01-012025-06-300000856982country:US2025-01-012025-06-300000856982mmsi:PeripheralInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:PeripheralInterventionMembercountry:USmmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:OEMMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:OEMMembersrt:RestatementAdjustmentMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:OEMMembercountry:USmmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:EndoscopyDevicesMemberus-gaap:NonUsMembermmsi:EndoscopySegmentMember2024-04-012024-06-300000856982mmsi:EndoscopyDevicesMembercountry:USmmsi:EndoscopySegmentMember2024-04-012024-06-300000856982mmsi:CustomProceduralSolutionsMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:CustomProceduralSolutionsMembercountry:USmmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:CardiacInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:CardiacInterventionMembercountry:USmmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982us-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:PeripheralInterventionMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:OEMMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:EndoscopyDevicesMembermmsi:EndoscopySegmentMember2024-04-012024-06-300000856982mmsi:CustomProceduralSolutionsMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:CardiacInterventionMembermmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982country:USmmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982us-gaap:NonUsMember2024-04-012024-06-300000856982country:US2024-04-012024-06-300000856982mmsi:PeripheralInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:PeripheralInterventionMembercountry:USmmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:OEMMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:OEMMembersrt:RestatementAdjustmentMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:OEMMembercountry:USmmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:EndoscopyDevicesMemberus-gaap:NonUsMembermmsi:EndoscopySegmentMember2024-01-012024-06-300000856982mmsi:EndoscopyDevicesMembercountry:USmmsi:EndoscopySegmentMember2024-01-012024-06-300000856982mmsi:CustomProceduralSolutionsMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:CustomProceduralSolutionsMembercountry:USmmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:CardiacInterventionMemberus-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:CardiacInterventionMembercountry:USmmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982us-gaap:NonUsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:PeripheralInterventionMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:OEMMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:EndoscopyDevicesMembermmsi:EndoscopySegmentMember2024-01-012024-06-300000856982mmsi:CustomProceduralSolutionsMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982mmsi:CardiacInterventionMembermmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982country:USmmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982us-gaap:NonUsMember2024-01-012024-06-300000856982country:US2024-01-012024-06-300000856982mmsi:ScholtenSurgicalInstrumentsIncMember2024-03-082024-03-080000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2025-01-012025-03-310000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-01-012024-03-310000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:RevenueFromContractWithCustomerMember2025-04-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:CostOfSalesMember2025-04-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:RevenueFromContractWithCustomerMember2025-01-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:CostOfSalesMember2025-01-012025-06-300000856982us-gaap:InterestRateSwapMemberus-gaap:CashFlowHedgingMemberus-gaap:InterestExpenseMember2024-04-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:RevenueFromContractWithCustomerMember2024-04-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:CostOfSalesMember2024-04-012024-06-300000856982us-gaap:InterestRateSwapMemberus-gaap:CashFlowHedgingMemberus-gaap:InterestExpenseMember2024-01-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:RevenueFromContractWithCustomerMember2024-01-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:CostOfSalesMember2024-01-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMember2025-04-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMember2025-01-012025-06-300000856982us-gaap:InterestRateSwapMemberus-gaap:CashFlowHedgingMember2024-04-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMember2024-04-012024-06-300000856982us-gaap:InterestRateSwapMemberus-gaap:CashFlowHedgingMember2024-01-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMember2024-01-012024-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2025-04-012025-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2025-04-012025-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-04-012025-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2025-01-012025-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2025-01-012025-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-01-012025-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2024-04-012024-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-04-012024-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-04-012024-06-300000856982us-gaap:AccumulatedTranslationAdjustmentMember2024-01-012024-06-300000856982us-gaap:AccumulatedOtherComprehensiveIncomeMember2024-01-012024-06-300000856982us-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-01-012024-06-300000856982us-gaap:RetainedEarningsMember2025-04-012025-06-300000856982us-gaap:RetainedEarningsMember2025-01-012025-03-310000856982us-gaap:RetainedEarningsMember2024-04-012024-06-300000856982us-gaap:RetainedEarningsMember2024-01-012024-03-310000856982us-gaap:FairValueInputsLevel1Memberus-gaap:FairValueMeasurementsRecurringMember2025-06-300000856982us-gaap:FairValueInputsLevel1Memberus-gaap:FairValueMeasurementsRecurringMember2024-12-310000856982mmsi:CreditAgreementMemberus-gaap:RevolvingCreditFacilityMember2023-06-060000856982mmsi:EndoscopySegmentMember2025-06-300000856982mmsi:CardiovascularSegmentMember2025-06-300000856982mmsi:EndoscopySegmentMember2024-12-310000856982mmsi:CardiovascularSegmentMember2024-12-310000856982us-gaap:FairValueInputsLevel2Memberus-gaap:FairValueMeasurementsRecurringMember2025-06-300000856982us-gaap:FairValueInputsLevel2Memberus-gaap:FairValueMeasurementsRecurringMember2024-12-310000856982srt:WeightedAverageMembermmsi:CookMedicalHoldingsLlcMember2024-11-010000856982srt:WeightedAverageMembermmsi:EndoGastricSolutionsIncMember2024-07-010000856982us-gaap:TrademarksMember2025-06-300000856982us-gaap:PatentsMember2025-06-300000856982us-gaap:OtherIntangibleAssetsMember2025-06-300000856982us-gaap:LicensingAgreementsMember2025-06-300000856982us-gaap:DistributionRightsMember2025-06-300000856982us-gaap:DevelopedTechnologyRightsMember2025-06-300000856982us-gaap:CustomerListsMember2025-06-300000856982us-gaap:TrademarksMember2024-12-310000856982us-gaap:PatentsMember2024-12-310000856982us-gaap:OtherIntangibleAssetsMember2024-12-310000856982us-gaap:LicensingAgreementsMember2024-12-310000856982us-gaap:DistributionRightsMember2024-12-310000856982us-gaap:DevelopedTechnologyRightsMember2024-12-310000856982us-gaap:CustomerListsMember2024-12-310000856982mmsi:SelioMedicalLimitedSelioMember2025-06-3000008569822025-03-310000856982mmsi:SelioMedicalLimitedSelioMember2024-12-3100008569822024-03-310000856982mmsi:ContingentConsiderationMember2025-06-300000856982mmsi:ContingentConsiderationMember2025-03-310000856982mmsi:ContingentConsiderationMember2024-12-310000856982mmsi:ContingentConsiderationMember2024-06-300000856982mmsi:ContingentConsiderationMember2024-03-310000856982mmsi:ContingentConsiderationMember2023-12-310000856982mmsi:ContingentConsiderationMember2025-04-012025-06-300000856982mmsi:ContingentConsiderationMember2025-01-012025-06-300000856982mmsi:ContingentConsiderationMember2024-04-012024-06-300000856982mmsi:ContingentConsiderationMember2024-01-012024-06-300000856982us-gaap:RestrictedStockUnitsRSUMember2025-01-012025-06-300000856982us-gaap:PerformanceSharesMember2025-01-012025-06-300000856982us-gaap:EmployeeStockOptionMember2025-01-012025-06-300000856982mmsi:CashSettledPerformanceSharesMember2025-01-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMember2025-06-300000856982us-gaap:PerformanceSharesMember2025-06-300000856982us-gaap:EmployeeStockOptionMember2025-06-300000856982mmsi:CashSettledPerformanceSharesMember2025-06-300000856982us-gaap:ForeignExchangeForwardMember2025-01-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:FairValueHedgingMemberus-gaap:NondesignatedMember2025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:DesignatedAsHedgingInstrumentMember2025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:FairValueHedgingMemberus-gaap:NondesignatedMember2024-12-310000856982us-gaap:ForeignExchangeForwardMemberus-gaap:CashFlowHedgingMemberus-gaap:DesignatedAsHedgingInstrumentMember2024-12-310000856982mmsi:WellsFargoFixedRateDerivativeContractThreeMemberus-gaap:InterestRateSwapMemberus-gaap:DesignatedAsHedgingInstrumentMember2019-12-310000856982us-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2025-04-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2025-01-012025-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2024-04-012024-06-300000856982us-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2024-01-012024-06-300000856982us-gaap:OtherNoncurrentLiabilitiesMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2025-06-300000856982mmsi:AccruedLiabilitiesCurrentMemberus-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2025-06-300000856982mmsi:AccruedLiabilitiesCurrentMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2025-06-300000856982us-gaap:OtherNoncurrentLiabilitiesMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2024-12-310000856982mmsi:AccruedLiabilitiesCurrentMemberus-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2024-12-310000856982mmsi:AccruedLiabilitiesCurrentMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2024-12-310000856982us-gaap:PrepaidExpensesAndOtherCurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2025-06-300000856982us-gaap:PrepaidExpensesAndOtherCurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2025-06-300000856982us-gaap:OtherNoncurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2025-06-300000856982us-gaap:PrepaidExpensesAndOtherCurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:NondesignatedMember2024-12-310000856982us-gaap:PrepaidExpensesAndOtherCurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2024-12-310000856982us-gaap:OtherNoncurrentAssetsMemberus-gaap:ForeignExchangeForwardMemberus-gaap:DesignatedAsHedgingInstrumentMember2024-12-310000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMemberus-gaap:CallOptionMember2023-12-310000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMember2023-12-310000856982mmsi:CreditAgreementMemberus-gaap:LoansPayableMember2023-06-060000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMemberus-gaap:CommonStockMember2025-06-300000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMemberus-gaap:CommonStockMember2023-12-310000856982us-gaap:ConvertibleNotesPayableMember2025-06-300000856982mmsi:CreditAgreementMember2025-06-300000856982us-gaap:ConvertibleNotesPayableMember2024-12-310000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedOtherComprehensiveIncomeMember2025-04-012025-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-04-012025-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedOtherComprehensiveIncomeMember2025-01-012025-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2025-01-012025-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedOtherComprehensiveIncomeMember2024-04-012024-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-04-012024-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedOtherComprehensiveIncomeMember2024-01-012024-06-300000856982us-gaap:ReclassificationOutOfAccumulatedOtherComprehensiveIncomeMemberus-gaap:AccumulatedGainLossNetCashFlowHedgeParentMember2024-01-012024-06-300000856982mmsi:EndoscopySegmentMember2025-04-012025-06-300000856982mmsi:CardiovascularSegmentMember2025-04-012025-06-300000856982mmsi:EndoscopySegmentMember2025-01-012025-06-300000856982mmsi:EndoscopySegmentMember2024-04-012024-06-300000856982mmsi:CardiovascularSegmentMember2024-04-012024-06-300000856982mmsi:EndoscopySegmentMember2024-01-012024-06-300000856982mmsi:CardiovascularSegmentMember2024-01-012024-06-300000856982us-gaap:FairValueInputsLevel2Member2025-06-300000856982us-gaap:CommonStockMember2025-06-300000856982us-gaap:CommonStockMember2025-03-310000856982us-gaap:CommonStockMember2024-12-310000856982us-gaap:CommonStockMember2024-06-300000856982us-gaap:CommonStockMember2024-03-310000856982us-gaap:CommonStockMember2023-12-3100008569822023-12-3100008569822024-06-300000856982mmsi:BiolifeLLCMemberus-gaap:TrademarksMember2025-05-160000856982mmsi:BiolifeLLCMemberus-gaap:DevelopedTechnologyRightsMember2025-05-160000856982mmsi:BiolifeLLCMemberus-gaap:CustomerListsMember2025-05-160000856982mmsi:CookMedicalHoldingsLlcMemberus-gaap:TrademarksMember2024-11-010000856982mmsi:CookMedicalHoldingsLlcMemberus-gaap:DevelopedTechnologyRightsMember2024-11-010000856982mmsi:CookMedicalHoldingsLlcMemberus-gaap:CustomerListsMember2024-11-010000856982mmsi:EndoGastricSolutionsIncMemberus-gaap:TrademarksMember2024-07-010000856982mmsi:EndoGastricSolutionsIncMemberus-gaap:DevelopedTechnologyRightsMember2024-07-010000856982mmsi:EndoGastricSolutionsIncMemberus-gaap:CustomerListsMember2024-07-010000856982srt:WeightedAverageMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2025-06-300000856982srt:MinimumMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2025-06-300000856982srt:MaximumMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2025-06-300000856982mmsi:RevenueMilestonesMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2025-06-300000856982srt:WeightedAverageMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982srt:MinimumMembermmsi:RevenueMilestonesMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982srt:MinimumMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982srt:MaximumMembermmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982mmsi:RevenueMilestonesMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982mmsi:RegulatoryApprovalMilestoneMemberus-gaap:FairValueInputsLevel3Memberus-gaap:MeasurementInputDiscountRateMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982mmsi:RegulatoryApprovalMilestoneMemberus-gaap:FairValueInputsLevel3Membermmsi:MilestonePaymentProbabilityMemberus-gaap:IncomeApproachValuationTechniqueMember2024-12-310000856982us-gaap:FairValueInputsLevel3Memberus-gaap:FairValueMeasurementsRecurringMember2025-06-300000856982us-gaap:EstimateOfFairValueFairValueDisclosureMemberus-gaap:FairValueMeasurementsRecurringMember2025-06-300000856982mmsi:RevenueMilestonesMemberus-gaap:FairValueInputsLevel3Member2025-06-300000856982mmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Member2025-06-300000856982us-gaap:FairValueInputsLevel3Memberus-gaap:FairValueMeasurementsRecurringMember2024-12-310000856982us-gaap:EstimateOfFairValueFairValueDisclosureMemberus-gaap:FairValueMeasurementsRecurringMember2024-12-310000856982mmsi:RevenueMilestonesMemberus-gaap:FairValueInputsLevel3Member2024-12-310000856982mmsi:RevenueBasedPaymentsMemberus-gaap:FairValueInputsLevel3Member2024-12-310000856982mmsi:RegulatoryApprovalMilestoneMemberus-gaap:FairValueInputsLevel3Member2024-12-310000856982mmsi:CookMedicalHoldingsLlcMember2024-11-012024-11-010000856982mmsi:EndoGastricSolutionsIncMember2024-07-012024-07-010000856982mmsi:BiolifeLLCMember2025-01-012025-06-300000856982mmsi:EndoGastricSolutionsIncMember2024-01-012024-12-310000856982mmsi:CookMedicalHoldingsLlcMember2024-01-012024-12-310000856982mmsi:ScholtenSurgicalInstrumentsIncMembermmsi:ContingentConsiderationPaymentTwoMember2024-03-082024-03-080000856982mmsi:ScholtenSurgicalInstrumentsIncMembermmsi:ContingentConsiderationPaymentThreeMember2024-03-082024-03-080000856982mmsi:ScholtenSurgicalInstrumentsIncMembermmsi:ContingentConsiderationPaymentOneMember2024-03-082024-03-080000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:ResearchAndDevelopmentExpenseMember2025-04-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:CostOfSalesMember2025-04-012025-06-300000856982us-gaap:PerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:ResearchAndDevelopmentExpenseMember2025-04-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:CostOfSalesMember2025-04-012025-06-300000856982mmsi:CashSettledRestrictedStockUnitsMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982mmsi:CashSettledPerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982us-gaap:SellingGeneralAndAdministrativeExpensesMember2025-04-012025-06-300000856982us-gaap:ResearchAndDevelopmentExpenseMember2025-04-012025-06-300000856982us-gaap:CostOfSalesMember2025-04-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:ResearchAndDevelopmentExpenseMember2025-01-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:CostOfSalesMember2025-01-012025-06-300000856982us-gaap:PerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:ResearchAndDevelopmentExpenseMember2025-01-012025-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:CostOfSalesMember2025-01-012025-06-300000856982mmsi:CashSettledRestrictedStockUnitsMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982mmsi:CashSettledPerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982us-gaap:SellingGeneralAndAdministrativeExpensesMember2025-01-012025-06-300000856982us-gaap:ResearchAndDevelopmentExpenseMember2025-01-012025-06-300000856982us-gaap:CostOfSalesMember2025-01-012025-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-04-012024-06-300000856982us-gaap:PerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-04-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-04-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:ResearchAndDevelopmentExpenseMember2024-04-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:CostOfSalesMember2024-04-012024-06-300000856982mmsi:CashSettledPerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-04-012024-06-300000856982us-gaap:SellingGeneralAndAdministrativeExpensesMember2024-04-012024-06-300000856982us-gaap:ResearchAndDevelopmentExpenseMember2024-04-012024-06-300000856982us-gaap:CostOfSalesMember2024-04-012024-06-300000856982us-gaap:RestrictedStockUnitsRSUMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-01-012024-06-300000856982us-gaap:PerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-01-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-01-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:ResearchAndDevelopmentExpenseMember2024-01-012024-06-300000856982us-gaap:EmployeeStockOptionMemberus-gaap:CostOfSalesMember2024-01-012024-06-300000856982mmsi:CashSettledPerformanceSharesMemberus-gaap:SellingGeneralAndAdministrativeExpensesMember2024-01-012024-06-300000856982us-gaap:SellingGeneralAndAdministrativeExpensesMember2024-01-012024-06-300000856982us-gaap:ResearchAndDevelopmentExpenseMember2024-01-012024-06-300000856982us-gaap:CostOfSalesMember2024-01-012024-06-3000008569822025-01-012025-03-3100008569822024-01-012024-03-310000856982us-gaap:CommonStockMember2025-01-012025-03-310000856982us-gaap:CommonStockMember2024-01-012024-03-310000856982srt:MaximumMembermmsi:CashSettledPerformanceSharesMember2025-01-012025-06-300000856982srt:ChiefExecutiveOfficerMembermmsi:CashSettledPerformanceSharesMember2025-01-012025-06-300000856982srt:MaximumMembermmsi:CashSettledPerformanceSharesMember2024-01-012024-06-300000856982srt:ChiefExecutiveOfficerMembermmsi:CashSettledPerformanceSharesMember2024-01-012024-06-300000856982srt:MaximumMembermmsi:CashSettledPerformanceSharesMember2025-01-012025-03-310000856982srt:MaximumMembermmsi:CashSettledPerformanceSharesMember2024-01-012024-03-310000856982mmsi:BiolifeLLCMember2025-05-162025-05-160000856982mmsi:CardiovascularSegmentMember2025-01-012025-06-300000856982mmsi:CreditAgreementMember2025-01-012025-06-300000856982srt:MinimumMemberus-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMember2023-12-012023-12-3100008569822025-06-3000008569822024-12-310000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMember2025-01-012025-06-300000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMemberus-gaap:CallOptionMember2023-12-012023-12-310000856982us-gaap:ConvertibleNotesPayableMembermmsi:SeniorUnsecuredConvertibleNotesMember2023-12-012023-12-310000856982mmsi:RevenueAndCostOfSalesMember2025-01-012025-06-300000856982mmsi:CookMedicalHoldingsLlcMember2024-11-010000856982mmsi:EndoGastricSolutionsIncMember2024-07-010000856982us-gaap:OtherNoncurrentLiabilitiesMember2025-06-300000856982us-gaap:OtherNoncurrentLiabilitiesMember2024-12-310000856982mmsi:AccruedLiabilitiesCurrentMember2025-06-300000856982mmsi:AccruedLiabilitiesCurrentMember2024-12-310000856982mmsi:BiolifeLLCMember2025-05-1600008569822024-04-012024-06-300000856982mmsi:ScholtenSurgicalInstrumentsIncMember2024-03-0800008569822024-01-012024-06-3000008569822025-04-012025-06-3000008569822025-07-2800008569822025-01-012025-06-30xbrli:sharesiso4217:USDmmsi:itemxbrli:pureiso4217:USDxbrli:sharesiso4217:USDmmsi:derivativemmsi:segment

Table of Contents

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

    QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended June 30, 2025

OR

    TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from                to                .

Commission File Number   0-18592

Graphic

MERIT MEDICAL SYSTEMS, INC.

(Exact name of registrant as specified in its charter)

Utah

    

87-0447695

(State or other jurisdiction of incorporation or organization)

(IRS Employer Identification No.)

1600 West Merit Parkway, South Jordan, Utah 84095

(Address of principal executive offices, including zip code)

Registrant’s telephone number, including area code: (801) 253-1600

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading Symbol

Name of exchange on which registered

Common Stock, no par value

MMSI

NASDAQ Global Select Market

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports) and (2) has been subject to filing requirements for the past 90 days. Yes   No

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes   No

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and "emerging growth company" in Rule 12b-2 of the Exchange Act.

Large Accelerated Filer 

Accelerated Filer 

Non-Accelerated Filer 

Smaller Reporting Company 

Emerging Growth Company 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes   No

Indicate the number of shares outstanding of each of the Registrant’s classes of common stock, as of the latest practicable date.

Title or class

Shares outstanding as of July 28, 2025

Common Stock, no par value

    

59,219,117

Table of Contents

TABLE OF CONTENTS

PART I.

   

FINANCIAL INFORMATION

3

Item 1.

Financial Statements (Unaudited)

3

Consolidated Balance Sheets

3

Consolidated Statements of Income

5

Consolidated Statements of Comprehensive Income

6

Consolidated Statements of Stockholders’ Equity

7

Consolidated Statements of Cash Flows

9

Condensed Notes to Consolidated Financial Statements

11

Item 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

33

Item 3.

Quantitative and Qualitative Disclosures About Market Risk

41

Item 4.

Controls and Procedures

42

PART II.

OTHER INFORMATION

43

Item 1.

Legal Proceedings

43

Item 1A.

Risk Factors

43

Item 5.

Other information

44

Item 6.

Exhibits

45

SIGNATURES

46

Table of Contents

PART I - FINANCIAL INFORMATION

ITEM 1. FINANCIAL STATEMENTS

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

(In thousands)

    

June 30, 

    

December 31, 

ASSETS

    

2025

    

2024

(unaudited)

Current assets:

 

  

 

  

Cash and cash equivalents

$

341,819

$

376,715

Trade receivables — net of allowance for credit losses — 2025 — $10,108 and 2024 — $9,729

 

204,162

 

190,243

Other receivables

 

14,292

 

16,588

Inventories

 

323,309

 

306,063

Prepaid expenses and other current assets

 

30,162

 

28,544

Prepaid income taxes

 

3,543

 

3,286

Income tax refund receivables

 

5,785

 

2,335

Total current assets

 

923,072

 

923,774

Property and equipment:

 

  

 

  

Land and land improvements

 

30,467

 

25,846

Buildings

 

198,505

 

192,296

Manufacturing equipment

 

353,119

 

340,864

Furniture and fixtures

 

64,102

 

61,321

Leasehold improvements

 

60,649

 

58,770

Construction-in-progress

 

74,850

 

58,673

Total property and equipment

 

781,692

 

737,770

Less accumulated depreciation

 

(371,707)

 

(351,605)

Property and equipment — net

 

409,985

386,165

Other assets:

 

  

 

  

Intangible assets:

 

  

 

  

Developed technology — net of accumulated amortization — 2025 — $414,713 and 2024 — $377,993

 

489,975

 

431,766

Other — net of accumulated amortization — 2025 — $90,872 and 2024 — $85,343

 

72,183

 

66,499

Goodwill

 

504,555

 

463,511

Deferred income tax assets

 

16,243

 

16,044

Right-of-use operating lease assets

89,279

65,508

Other assets

 

80,753

 

65,336

Total other assets

 

1,252,988

 

1,108,664

Total assets

$

2,586,045

$

2,418,603

See condensed notes to consolidated financial statements.

(continued)

3

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

(In thousands)

    

June 30, 

    

December 31, 

LIABILITIES AND STOCKHOLDERS’ EQUITY

    

2025

    

2024

(unaudited)

Current liabilities:

 

  

  

Trade payables

$

69,066

$

68,502

Accrued expenses

 

140,204

 

134,077

Short-term operating lease liabilities

10,262

10,331

Income taxes payable

 

6,040

 

3,492

Total current liabilities

 

225,572

 

216,402

Long-term debt

 

731,795

 

729,551

Deferred income tax liabilities

 

26,925

 

240

Liabilities related to unrecognized tax benefits

 

2,169

 

2,118

Deferred compensation payable

 

19,800

 

19,197

Deferred credits

 

1,450

 

1,502

Long-term operating lease liabilities

78,496

 

54,783

Other long-term obligations

 

11,790

 

15,451

Total liabilities

 

1,097,997

 

1,039,244

Commitments and contingencies

 

  

 

  

Stockholders' equity:

 

  

 

  

Preferred stock — 5,000 shares authorized; no shares issued as of June 30, 2025 and December 31, 2024

 

 

Common stock, no par value — 100,000 shares authorized; issued and outstanding as of June 30, 2025 - 59,218 and December 31, 2024 - 58,743

 

734,841

 

703,219

Retained earnings

 

758,269

 

695,541

Accumulated other comprehensive loss

 

(5,062)

 

(19,401)

Total stockholders’ equity

 

1,488,048

 

1,379,359

Total liabilities and stockholders’ equity

$

2,586,045

$

2,418,603

See condensed notes to consolidated financial statements.

(concluded)

4

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF INCOME

(In thousands, except per share amounts - unaudited)

    

Three Months Ended

    

Six Months Ended

June 30, 

June 30, 

    

2025

    

2024

    

2025

    

2024

Net sales

$

382,462

$

338,003

$

737,813

$

661,511

Cost of sales

 

197,975

 

176,903

 

381,306

 

348,696

Gross profit

 

184,487

 

161,100

 

356,507

 

312,815

Operating expenses:

 

  

 

  

 

  

 

  

Selling, general and administrative

 

113,097

 

94,585

 

220,583

 

189,013

Research and development

 

24,367

 

20,263

 

46,845

 

41,745

Contingent consideration expense

 

143

 

306

 

1,166

 

189

Total operating expenses

 

137,607

 

115,154

 

268,594

 

230,947

Income from operations

 

46,880

 

45,946

 

87,913

 

81,868

Other income (expense):

 

  

 

  

 

  

 

  

Interest income

 

3,761

 

7,561

 

7,551

 

14,837

Interest expense

 

(6,775)

 

(7,679)

 

(13,343)

 

(15,725)

Other (expense) income — net

 

(487)

 

15

 

(784)

 

(789)

Total other expense — net

 

(3,501)

 

(103)

 

(6,576)

 

(1,677)

Income before income taxes

 

43,379

 

45,843

 

81,337

 

80,191

Income tax expense

 

10,798

 

10,117

 

18,609

 

16,225

Net income

$

32,581

$

35,726

$

62,728

$

63,966

Earnings per common share

 

  

 

  

 

  

 

  

Basic

$

0.55

$

0.61

$

1.06

$

1.10

Diluted

$

0.54

$

0.61

$

1.03

$

1.09

Weighted average shares outstanding

 

  

 

  

 

  

 

  

Basic

 

59,140

 

58,139

 

59,019

 

58,049

Diluted

 

60,611

 

58,740

 

60,945

 

58,653

See condensed notes to consolidated financial statements.

5

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME

(In thousands - unaudited)

    

Three Months Ended

    

Six Months Ended

June 30, 

June 30, 

    

2025

    

2024

    

2025

    

2024

Net income

$

32,581

$

35,726

$

62,728

$

63,966

Other comprehensive income (loss):

 

  

 

  

 

  

 

  

Cash flow hedges

 

(1,663)

 

(1,711)

 

(4,049)

 

1,261

Income tax benefit (expense)

 

393

 

404

 

956

 

(298)

Foreign currency translation adjustment

 

13,200

 

(1,688)

 

19,054

 

(5,092)

Income tax benefit (expense)

 

(1,616)

 

22

 

(1,622)

 

34

Total other comprehensive income (loss)

 

10,314

 

(2,973)

 

14,339

 

(4,095)

Total comprehensive income

$

42,895

$

32,753

$

77,067

$

59,871

See condensed notes to consolidated financial statements.

6

Table of Contents

MERIT MEDICAL SYSTEMS, INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

(In thousands - unaudited)

Common Stock

Retained

Accumulated Other

    

Shares

    

Amount

    

Earnings

    

Comprehensive Loss

    

Total

Balance — January 1, 2025

 

58,743

$

703,219

$

695,541

$

(19,401)

$

1,379,359

Net income

 

  

 

  

 

30,147

 

  

 

30,147

Other comprehensive income

 

  

 

  

 

  

 

4,025

 

4,025

Stock-based compensation expense

 

  

 

7,885

 

  

 

  

 

7,885

Options exercised

 

281

 

14,610

 

  

 

  

 

14,610

Issuance of common stock under Employee Stock Purchase Plan

 

4

 

424

 

  

 

  

 

424

Shares issued from time-vested restricted stock units

130

Shares surrendered in exchange for payment of payroll tax liabilities

 

(62)

(6,145)

(6,145)

Shares surrendered in exchange for exercise of stock options

 

(18)

 

(1,882)

(1,882)

Balance — March 31, 2025

 

59,078

718,111

725,688

(15,376)

1,428,423

Net income

 

  

 

  

 

32,581

 

  

 

32,581

Other comprehensive income

 

  

 

  

 

  

 

10,314

 

10,314

Stock-based compensation expense

 

  

 

9,868

 

  

 

  

 

9,868

Options exercised

 

114

 

6,523

 

  

 

  

 

6,523

Issuance of common stock under Employee Stock Purchase Plan

 

4

 

339

 

  

 

  

 

339

Shares issued from time-vested restricted stock units

22

Balance — June 30, 2025

 

59,218

$

734,841

$

758,269

$

(5,062)

$

1,488,048

See condensed notes to consolidated financial statements.

(continued)

7

Table of Contents

MERIT MEDICAL SYSTEMS, INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

(In thousands - unaudited)

Common Stock

Retained

Accumulated Other

    

Shares

    

Amount

    

Earnings

    

Comprehensive Loss

    

Total

Balance — January 1, 2024

 

57,858

$

638,150

$

575,184

$

(11,334)

$

1,202,000

Net income

 

  

 

  

 

28,240

 

  

 

28,240

Other comprehensive loss

 

 

 

 

(1,122)

 

(1,122)

Stock-based compensation expense

 

 

4,934

 

 

 

4,934

Options exercised

 

213

 

7,394

 

 

 

7,394

Issuance of common stock under Employee Stock Purchase Plan

 

5

 

336

 

 

 

336

Shares issued from time-vested restricted stock units

47

Shares surrendered in exchange for payment of payroll tax liabilities

 

(21)

 

(1,592)

(1,592)

Balance — March 31, 2024

 

58,102

649,222

603,424

(12,456)

1,240,190

Net income

 

  

 

  

 

35,726

 

  

 

35,726

Other comprehensive loss

 

  

 

  

 

  

 

(2,973)

 

(2,973)

Stock-based compensation expense

 

 

6,301

 

  

 

  

 

6,301

Options exercised

 

66

 

2,913

 

  

 

  

 

2,913

Issuance of common stock under Employee Stock Purchase Plan

 

4

 

288

 

  

 

  

 

288

Shares issued from time-vested restricted stock units

20

Balance — June 30, 2024

58,192

$

658,724

$

639,150

$

(15,429)

$

1,282,445

See condensed notes to consolidated financial statements.

(concluded)

8

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands - unaudited)

Six Months Ended

June 30, 

    

2025

    

2024

CASH FLOWS FROM OPERATING ACTIVITIES:

 

Net income

$

62,728

$

63,966

Adjustments to reconcile net income to net cash provided by operating activities:

 

  

 

  

Depreciation and amortization

 

60,313

 

47,690

Gain on disposition of business

 

(249)

 

Loss on sale or abandonment of property and equipment

 

315

 

79

Write-off of certain intangible assets and other long-term assets

 

82

 

280

Amortization of right-of-use operating lease assets

5,766

6,063

Fair value adjustments related to contingent consideration liabilities

1,166

189

Amortization of deferred credits

 

(52)

 

(52)

Amortization and write-off of long-term debt issuance costs

 

2,828

 

2,954

Stock-based compensation expense

 

19,951

 

12,245

Changes in operating assets and liabilities, net of acquisitions:

 

 

Trade receivables

 

(7,310)

 

(6,901)

Other receivables

 

2,817

 

(499)

Inventories

 

(11,720)

 

3,119

Prepaid expenses and other current assets

 

(2,575)

 

(2,306)

Income tax refund receivables

 

(3,653)

 

(3,621)

Other assets

 

(1,471)

 

(2,968)

Trade payables

 

3,697

 

(7,096)

Accrued expenses

 

(2,740)

 

(2,804)

Income taxes payable

 

1,537

 

(3,869)

Deferred compensation payable

 

603

 

1,421

Operating lease liabilities

(5,925)

(5,962)

Other long-term obligations

 

(2,229)

 

2,794

Total adjustments

 

61,151

 

40,756

Net cash, cash equivalents, and restricted cash provided by operating activities

 

123,879

 

104,722

CASH FLOWS FROM INVESTING ACTIVITIES:

 

  

 

  

Capital expenditures for:

 

  

 

  

Property and equipment

 

(34,812)

 

(22,309)

Intangible assets

 

(1,296)

 

(1,576)

Proceeds from the sale of property and equipment

 

45

 

2

Proceeds from disposition of business

249

Cash paid for notes receivable and other investments

 

(14,617)

 

(9,723)

Cash paid in acquisitions, net of cash acquired

 

(122,555)

 

(4,932)

Net cash, cash equivalents, and restricted cash used in investing activities

$

(172,986)

$

(38,538)

See condensed notes to consolidated financial statements.

(continued)

9

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands - unaudited)

    

Six Months Ended

June 30, 

2025

2024

CASH FLOWS FROM FINANCING ACTIVITIES:

 

Proceeds from issuance of common stock

$

20,014

$

10,931

Payments on long-term debt

(24,063)

Contingent payments related to acquisitions

 

(2,567)

 

(142)

Payment of taxes related to an exchange of common stock

 

(6,145)

 

(1,592)

Net cash, cash equivalents, and restricted cash provided by (used in) financing activities

 

11,302

 

(14,866)

Effect of exchange rates on cash, cash equivalents, and restricted cash

 

2,953

 

(1,750)

Net (decrease) increase in cash, cash equivalents and restricted cash

 

(34,852)

 

49,568

CASH, CASH EQUIVALENTS AND RESTRICTED CASH:

 

  

 

  

Beginning of period

378,767

589,144

End of period

$

343,915

$

638,712

RECONCILIATION OF CASH, CASH EQUIVALENTS AND RESTRICTED CASH TO THE CONSOLIDATED BALANCE SHEETS:

Cash and cash equivalents

341,819

636,658

Restricted cash reported in prepaid expenses and other current assets

2,096

2,054

Total cash, cash equivalents and restricted cash

$

343,915

$

638,712

SUPPLEMENTAL DISCLOSURES OF CASH FLOW INFORMATION

 

  

 

  

Cash paid during the period for:

 

  

 

  

Interest (net of capitalized interest of $594 and $428, respectively)

$

13,530

$

4,404

Income taxes

19,658

22,619

SUPPLEMENTAL DISCLOSURES OF NON-CASH INVESTING AND FINANCING ACTIVITIES

 

  

 

  

Property and equipment purchases in accounts payable

$

9,062

$

5,411

Acquisition purchases in accrued expenses and other long-term obligations

4,068

4,553

Merit common stock surrendered (18 and 0 shares, respectively) in exchange for exercise of stock options

1,882

Right-of-use operating lease assets obtained in exchange for operating lease liabilities

28,504

8,167

See condensed notes to consolidated financial statements.

(concluded)

10

Table of Contents

MERIT MEDICAL SYSTEMS, INC. AND SUBSIDIARIES

CONDENSED NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(Unaudited)

1.   Basis of Presentation and Other Items. The interim consolidated financial statements of Merit Medical Systems, Inc. ("Merit," "we" or "us") for the three and six-month periods ended June 30, 2025 and 2024 are not audited. Our consolidated financial statements are prepared in accordance with the requirements for unaudited interim periods and, consequently, do not include all disclosures required to be made in conformity with accounting principles generally accepted in the United States of America. In the opinion of our management, the accompanying consolidated financial statements contain all adjustments, consisting of normal recurring accruals, necessary for a fair presentation of our financial position, results of operations and cash flows for the periods presented in conformity with GAAP. The results of operations presented in these interim consolidated financial statements are not necessarily indicative of the results for a full-year period. Amounts presented in this report are rounded, while percentages and earnings per share amounts presented are calculated from the underlying amounts. These interim consolidated financial statements should be read in conjunction with the financial statements and risk factors included in our Annual Report on Form 10-K for the year ended December 31, 2024 (the “2024 Annual Report on Form 10-K”).

We elected to change the presentation of investments in privately held companies within the statements of cash flows to be included within Cash paid for notes receivable and other investments. Previously, amounts paid to acquire such investments were presented within Cash paid in acquisitions, net of cash acquired. The change in presentation had no material impact on previously reported financial information and comparative periods have been adjusted to reflect this change in presentation.

2.   Recently Issued Accounting Standards. In December 2023, the Financial Accounting Standards Board (“FASB”) issued Accounting Standard Update (“ASU”) 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, to improve annual basis income tax disclosures related to (1) rate reconciliation, (2) income taxes paid, and (3) other disclosures related to pretax income (or loss) and income tax expense (or benefit) from continuing operations. ASU 2023-09 is effective for fiscal years beginning after December 15, 2024, with early adoption permitted. These amendments are to be applied on a prospective basis. Retrospective application is permitted. We are currently evaluating the impact this standard will have on our consolidated financial statement disclosures.

In November 2024, the FASB issued ASU 2024-03, Disaggregation of Income Statement Expenses, which requires a public entity to disclose certain operating expenses disaggregated into categories, such as purchases of inventory, employee compensation, depreciation, and intangible asset amortization on an annual and interim basis. ASU 2024-03 is effective for fiscal years beginning after December 15, 2026, and interim periods within fiscal years beginning after December 15, 2027, with early adoption permitted. The provisions within the update may be applied retrospectively for all periods presented in the financial statements. While we are still evaluating the specific impacts and adoption method, we anticipate this guidance will have a significant impact on our consolidated financial statement disclosures.

11

Table of Contents

3.   Revenue from Contracts with Customers. We recognize revenue when a customer obtains control of promised goods. The amount of revenue recognized reflects the consideration we expect to receive in exchange for these goods. Our revenue recognition policies have not changed from those disclosed in Note 1 to our consolidated financial statements in Item 8 of the 2024 Annual Report on Form 10-K.

Disaggregation of Revenue

Our revenue is disaggregated based on reporting segment, product category and geographic region. We design, develop, manufacture and market medical products for interventional, diagnostic and therapeutic procedures. For financial reporting purposes, we report our operations in two operating segments: cardiovascular and endoscopy. Our cardiovascular segment consists of four product categories: peripheral intervention, cardiac intervention, custom procedural solutions, and original equipment manufacturer (“OEM”). Within these product categories, we sell a variety of products, including cardiology and radiology devices (which assist in diagnosing and treating coronary arterial disease, peripheral vascular disease and other non-vascular diseases), as well as embolotherapeutic, cardiac rhythm management, electrophysiology, critical care, breast cancer localization and guidance, biopsy, and interventional oncology and spine devices. Our endoscopy segment consists of gastroenterology and pulmonology devices which assist in the palliative treatment of expanding esophageal, tracheobronchial and biliary strictures.

The following tables present revenue from contracts with customers by reporting segment, product category and geographic region for the three and six-month periods ended June 30, 2025 and 2024 (in thousands):

Three Months Ended

Three Months Ended

June 30, 2025

June 30, 2024*

    

United States

    

International

    

Total

    

United States

    

International

    

Total

Cardiovascular

 

  

 

 

  

 

  

 

  

 

  

Peripheral Intervention

$

83,987

$

58,860

$

142,847

$

77,627

$

56,759

$

134,386

Cardiac Intervention

 

46,100

69,151

 

115,251

 

36,830

56,477

 

93,307

Custom Procedural Solutions

 

32,710

20,924

 

53,634

 

30,454

19,678

 

50,132

OEM

 

46,932

5,361

 

52,293

 

40,241

9,749

 

49,990

Total

 

209,729

154,296

 

364,025

 

185,152

 

142,663

 

327,815

 

Endoscopy

Endoscopy Devices

 

17,353

 

1,084

 

18,437

 

9,512

 

676

 

10,188

Total

$

227,082

$

155,380

$

382,462

$

194,664

$

143,339

$

338,003

Six Months Ended

Six Months Ended

June 30, 2025

June 30, 2024*

   

United States

   

International

   

Total

   

United States

   

International

   

Total

Cardiovascular

 

 

 

  

 

  

 

  

 

  

Peripheral Intervention

$

164,144

$

115,982

$

280,126

$

152,431

$

112,021

$

264,452

Cardiac Intervention

 

87,499

127,493

 

214,992

 

72,167

111,316

 

183,483

Custom Procedural Solutions

 

61,938

39,638

 

101,576

 

59,708

38,947

 

98,655

OEM

 

93,960

12,084

 

106,044

 

77,391

17,208

 

94,599

Total

 

407,541

295,197

 

702,738

 

361,697

 

279,492

 

641,189

 

Endoscopy

Endoscopy Devices

 

33,105

 

1,970

 

35,075

 

19,061

 

1,261

 

20,322

Total

$

440,646

$

297,167

$

737,813

$

380,758

$

280,753

$

661,511

*Commencing January 1, 2025, we reorganized our sales teams and product categories to include revenues from the sale of our spine devices under our OEM product category. Revenue figures for 2024 have been recast to reflect this realignment of our portfolio of spine products, representing approximately $5.7 million and $11.0 million in revenue for the three and six-month periods ended June 30, 2024, within the OEM product category to provide comparability between the reported periods.

12

Table of Contents

4.   Acquisitions and Investments. On May 16, 2025, Merit entered into an Agreement and Plan of Merger (the “Biolife Agreement”) by and among, Merit, Biolife, L.L.C., a Florida limited liability company (“FL Biolife”), Biolife Transaction Sub, LLC, a Delaware limited liability company (“Merger Sub”), and Shareholder Representative Services LLC, a Colorado limited liability company. Promptly following the execution of the Biolife Agreement, FL Biolife converted from a Florida limited liability company to a Delaware limited liability company called Biolife Delaware, L.L.C. (“Biolife”). Pursuant to the terms of the Biolife Agreement, on May 20, 2025, Merger Sub merged with and into Biolife, with Biolife continuing as the surviving corporation and a wholly-owned subsidiary of Merit (the “Biolife Merger”). The purchase consideration consisted of an upfront payment of $120 million plus working capital and other adjustments of $6.3 million in cash. Biolife manufactures unique patented hemostatic devices under the brand names StatSeal and WoundSeal. We accounted for the Biolife Merger as a business combination. During the six-month period ended June 30, 2025, our net sales of Biolife products were approximately $1.4 million. It is not practical to separately report earnings related to the products acquired in connection with the Biolife Merger, as we cannot split our sales costs related solely to the Biolife products, principally because our sales representatives sell multiple products (including the Biolife products) in our cardiovascular business segment. Acquisition-related costs associated with the Biolife Merger, which are included in selling, general and administrative expenses in the accompanying consolidated statements of income, were approximately $2.0 million for the six-month period ended June 30, 2025. The following table summarizes the preliminary purchase price allocated to the net assets acquired in connection with the Biolife Merger (in thousands):

Assets Acquired

    

  

Cash and cash equivalents

$

7,380

Trade receivables

1,562

Inventories

1,748

Prepaid expenses and other current assets

172

Property and equipment

4,609

Intangible assets

 

Developed technology

92,700

Trademarks

3,800

Customer list

4,600

Goodwill

38,286

Total assets acquired

 

154,857

Liabilities Assumed

 

  

Trade payables

133

Accrued expenses

1,551

Income taxes payable

26

Deferred income tax liabilities

26,661

Liabilities related to unrecognized tax benefits

51

Other long-term obligations

 

139

Total liabilities assumed

 

28,561

Total assets acquired, net of liabilities assumed

126,296

Less: Cash acquired

(7,380)

Purchase price, net of cash acquired

$

118,916

We are amortizing the Biolife developed technology intangible assets over 12 years, the trademark intangible assets over 12 years, and the customer list intangible asset on an accelerated basis over 12 years. We have estimated the weighted average life of the intangible assets acquired from Biolife to be 12 years. The goodwill consists largely of the synergies expected from combining operations and is not expected to be deductible for tax purposes. The pro forma effects to our consolidated results of operations of the Biolife Acquisition are not material in relation to reported sales.

13

Table of Contents

On November 1, 2024, pursuant to the terms of the Asset Purchase Agreement (the “Cook Purchase Agreement”) dated September 18, 2024 between Merit and Cook Medical Holdings LLC, (“Cook”), we acquired Cook’s lead management business, which is composed of a comprehensive end-to-end portfolio of medical devices and accessories used in lead management procedures for patients who need a pacemaker or an implantable cardioverter-defibrillator lead removed or replaced. We acquired the portfolio for a purchase price of $210 million, plus the assumption of certain liabilities. We accounted for this transaction under the acquisition method of accounting as a business combination. Acquisition-related costs associated with the transaction, which were included in selling, general and administrative expenses in the consolidated statements of income included in the 2024 Annual Report on Form 10-K were approximately $5.4 million during the year ended December 31, 2024. The purchase price was allocated as follows (in thousands):

Assets Acquired

    

  

Intangible assets

 

Developed technology

$

126,100

Trademarks

7,100

Customer list

11,100

Goodwill

65,897

Total assets acquired

 

210,197

Liabilities Assumed

 

  

Accrued expenses

 

197

Total liabilities assumed

 

197

Total net assets acquired

$

210,000

We are amortizing the Cook developed technology intangible assets over ten years, the trademark intangible assets over 12 years, and the customer list intangible asset on an accelerated basis over 12 years. We have estimated the weighted average life of the intangible assets acquired from Cook to be 10.3 years. The goodwill consists largely of the synergies expected from combining operations and is expected to be deductible for income tax purposes. The pro forma effects on our consolidated results of operations of the Cook acquisition are not material in relation to reported sales and it was deemed impracticable to obtain information to determine earnings associated with the acquired product lines which represent only a small portion of the product lines of a large, consolidated company without standalone financial information.

14

Table of Contents

On July 1, 2024, we entered into an Asset Purchase Agreement (the “EGS Purchase Agreement”) with EndoGastric Solutions, Inc. (“EGS”), pursuant to which we acquired the EsophyX® Z+ device and various assets related thereto (collectively, the “EGS Acquisition”), which are designed to deliver a durable, minimally invasive non-pharmacological treatment option for patients suffering from gastroesophageal reflux disease. We acquired the purchased assets identified under the EGS Purchase Agreement for a purchase price of $105 million. We accounted for the EGS Acquisition under the acquisition method of accounting as a business combination. The sales related to the EGS Acquisition have been included in our endoscopy segment since the acquisition date. Acquisition-related costs associated with the EGS Acquisition, which were included in selling, general and administrative expenses in the consolidated statements of income included in the 2024 Annual Report on Form 10-K were approximately $3.4 million during the year ended December 31, 2024. The purchase price was allocated as follows (in thousands):

Assets Acquired

    

  

Trade receivables

$

2,568

Inventories

3,553

Prepaid expenses and other current assets

99

Property and equipment

258

Intangible assets

 

Developed technology

72,800

Trademarks

5,400

Customer list

6,600

Goodwill

16,997

Total assets acquired

 

108,275

Liabilities Assumed

 

  

Trade payables

 

494

Accrued expenses

 

2,752

Total liabilities assumed

 

3,246

Total net assets acquired

$

105,029

We are amortizing the EGS developed technology intangible assets over ten years, the trademark intangible assets over 11 years, and the customer list intangible asset on an accelerated basis over 11 years. We have estimated the weighted average life of the intangible assets acquired from EGS to be 10.1 years. The goodwill consists largely of the synergies expected from combining operations and is expected to be deductible for income tax purposes. The pro forma effects to our consolidated results of operations of the EGS Acquisition are not material in relation to reported sales.

On March 8, 2024, we entered into an asset purchase agreement with Scholten Surgical Instruments, Inc. (“SSI”) to acquire the assets associated with the Bioptome, Novatome, and Sensatome devices. The total purchase price of the SSI assets included an up-front payment of $3 million, and three deferred payments, including (i) $1 million payable upon the earlier of (a) the first anniversary of the closing date or (b) the date on which Merit can independently manufacture the purchased devices (“Deferred Payment Date”), (ii) $1 million payable upon the first anniversary of the Deferred Payment Date, and (iii) $1 million payable upon the second anniversary of the Deferred Payment Date. We have accounted for this transaction as an asset purchase, and recorded the amount paid and deferred payments as a developed technology intangible asset, which we are amortizing over eight years.

5. Inventories. Inventories at June 30, 2025 and December 31, 2024 consisted of the following (in thousands):

    

June 30, 2025

    

December 31, 2024

Finished goods

$

170,277

$

168,437

Work-in-process

 

36,030

 

27,114

Raw materials

 

117,002

 

110,512

Total inventories

$

323,309

$

306,063

15

Table of Contents

6.   Goodwill and Intangible Assets. The change in the carrying amount of goodwill by segment for the six-month period ended June 30, 2025 is detailed as follows (in thousands):

2025

    

Cardiovascular

Endoscopy

Total

Goodwill balance at January 1

$

446,514

$

16,997

$

463,511

Effect of foreign exchange

 

2,758

 

 

2,758

Additions and adjustments as the result of acquisitions

 

38,286

 

 

38,286

Goodwill balance at June 30

$

487,558

$

16,997

$

504,555

Total accumulated goodwill impairment losses aggregated to $8.3 million as of June 30, 2025 and December 31, 2024, respectively. We did not have any goodwill impairments for the three and six-month periods ended June 30, 2025 or 2024.

Other intangible assets at June 30, 2025 and December 31, 2024 consisted of the following (in thousands):

June 30, 2025

Gross Carrying

Accumulated

Net Carrying

    

Amount

    

Amortization

    

Amount

Patents

$

33,078

$

(13,786)

$

19,292

Distribution agreements

 

3,250

 

(3,031)

 

219

License agreements

 

12,595

 

(9,608)

 

2,987

Trademarks

 

51,456

 

(26,233)

 

25,223

Customer lists

 

62,676

 

(38,214)

 

24,462

Total

$

163,055

$

(90,872)

$

72,183

December 31, 2024

Gross Carrying

Accumulated

Net Carrying

    

Amount

    

Amortization

    

Amount

Patents

$

31,489

$

(12,824)

$

18,665

Distribution agreements

 

3,250

 

(2,994)

 

256

License agreements

 

11,557

 

(9,125)

 

2,432

Trademarks

 

47,613

 

(24,177)

 

23,436

Customer lists

 

57,933

 

(36,223)

 

21,710

Total

$

151,842

$

(85,343)

$

66,499

Aggregate amortization expense for developed technology and other intangible assets for the three and six-month periods ended June 30, 2025 was $21.5 million and $41.5 million, respectively. Aggregate amortization expense for the three and six-month periods ended June 30, 2024 was $14.8 million and $29.4 million, respectively.

We evaluate long-lived assets, including amortizing intangible assets, for impairment whenever events or changes in circumstances indicate that their carrying amounts may not be recoverable. We perform the impairment analysis at the asset group for which the lowest level of identifiable cash flows is largely independent of the cash flows of other assets and liabilities. If a triggering event is identified, we determine the fair value of our amortizing assets based on estimated future cash flows discounted back to their present value using a discount rate that reflects the risk profiles of the underlying activities. We did not identify indicators of impairment for our intangible assets based on our consideration of triggering events for the six-month periods ended June 30, 2025 and 2024, respectively.

16

Table of Contents

Estimated amortization expense for developed technology and other intangible assets for the next five years consisted of the following as of June 30, 2025 (in thousands):

Year ending December 31, 

    

Estimated Amortization Expense

Remaining 2025

$

45,989

2026

 

81,813

2027

 

78,208

2028

76,670

2029

 

65,166

7.   Income Taxes. Our provision for income taxes for the three-month periods ended June 30, 2025 and 2024 was a tax expense of $10.8 million and $10.1 million, respectively, which resulted in an effective tax rate of 24.9% and 22.1%, respectively. Our provision for income taxes for the six-month periods ended June 30, 2025 and 2024 was a tax expense of $18.6 million and $16.2 million, respectively, which resulted in an effective tax rate of 22.9% and 20.2%, respectively. The increase in the effective income tax rate and income tax expense for the three and six-month periods ended June 30, 2025, when compared to the prior-year periods, was primarily due to decreased benefit from discrete items such as share-based compensation and contingent liabilities and increased permanent tax differences in foreign jurisdictions. Our effective tax rate differs from the U.S. statutory rate primarily due to the impact of global intangible low-taxed income (“GILTI”) inclusions, state income taxes, foreign taxes, other nondeductible permanent items and discrete items (such as share-based compensation).

The Organization for Economic Cooperation and Development (“OECD”) Pillar Two global minimum tax rules, which generally provide for a minimum effective tax rate of 15%, were intended to apply for tax years beginning in 2024. On February 2, 2023, the OECD issued administrative guidance providing transition and safe harbor rules around the implementation of the Pillar Two global minimum tax. Under a transitional safe harbor released July 17, 2023, the undertaxed profits rule top-up tax in the jurisdiction of a company's ultimate parent entity will be zero for each fiscal year of the transition period, if that jurisdiction has a corporate tax rate of at least 20%. The safe harbor transition period will apply to fiscal years beginning on or before December 31, 2025 and ending before December 31, 2026. While we expect our effective income tax rate and cash income tax payments could increase in future years as a result of the global minimum tax, we do not anticipate a material impact to our fiscal 2025 consolidated results of operations. Our assessment could be affected by legislative guidance and future enactment of additional provisions within the Pillar Two framework. We are closely monitoring developments and evaluating the impact these new rules are anticipated to have on our tax rate, including eligibility to qualify for these safe harbor rules.

On July 4, 2025, the U.S. enacted a budget reconciliation package (known as the “One Big Beautiful Bill Act” or “OBBBA”) which includes a broad range of tax provisions affecting businesses. As the legislation was signed into law after the close of our second quarter, the impacts are not included in our operating results for the six months ended June 30, 2025, in accordance with ASC 740, Income Taxes. The Company is currently evaluating the impact of the new legislation and its impact on the consolidated financial statements. We currently do not expect the OBBBA to have a material impact on our estimated annual effective tax rate in 2025.

17

Table of Contents

8.   Debt. Principal balances outstanding under our long-term debt obligations as of June 30, 2025 and December 31, 2024 consisted of the following (in thousands):

    

June 30, 2025

    

December 31, 2024

Convertible notes

747,500

747,500

Less unamortized debt issuance costs

 

(15,705)

 

(17,949)

Total long-term debt

 

731,795

 

729,551

Less current portion

 

 

Long-term portion

$

731,795

$

729,551

Future minimum principal payments on our long-term debt, as of June 30, 2025, were as follows (in thousands):

Year Ending

Future Minimum

December 31,

    

Principal Payments

Remaining 2025

 

$

2026

2027

2028

2029

747,500

Total future minimum principal payments

$

747,500

Fourth Amended and Restated Credit Agreement

On June 6, 2023, we entered into a Fourth Amended and Restated Credit Agreement (the "Fourth A&R Credit Agreement"). The Fourth A&R Credit Agreement is a syndicated loan agreement with Wells Fargo Bank, National Association and other parties. The Fourth A&R Credit Agreement amended and restated in its entirety our previously outstanding Third Amended and Restated Credit Agreement and all amendments thereto. The Fourth A&R Credit Agreement provides for a term loan of $150 million and a revolving credit commitment of up to an aggregate amount of $700 million, inclusive of sub-facilities for multicurrency borrowings, standby letters of credit and swingline loans. On June 6, 2028, all principal, interest and other amounts outstanding under the Fourth A&R Credit Agreement are payable in full. At any time prior to the maturity date, we may repay any amounts owing under all term loans and revolving credit loans in whole or in part, without premium or penalty.

On December 5, 2023, we executed an amendment to the Fourth A&R Credit Agreement (as amended, the "Amended Fourth A&R Credit Agreement”) to facilitate the issuance of our Convertible Notes described below. Among other things, the amendment also updated the definition of the Applicable Margin used in determining the interest rates and amended the financial covenants, all as described below.

Term loans made under the Amended Fourth A&R Credit Agreement bear interest, at our election, at either (i) the Base Rate plus the Applicable Margin (as defined in the Amended Fourth A&R Credit Agreement) or, (ii) Adjusted Term SOFR plus the Applicable Margin (as defined in the Amended Fourth A&R Credit Agreement). Revolving credit loans bear interest, at our election, at either (a) the Base Rate plus the Applicable Margin, (b) Adjusted Term SOFR plus the Applicable Margin, (c) Adjusted Eurocurrency Rate plus the Applicable Margin (as defined in the Amended Fourth A&R Credit Agreement), or (d) Adjusted Daily Simple SONIA plus the Applicable Margin (as defined in the Amended Fourth A&R Credit Agreement). Swingline loans bear interest at the Base Rate plus the Applicable Margin. Interest on each loan featuring the Base Rate and each Daily Simple SONIA Loan is due and payable on the last business day of each calendar month; interest on each loan featuring the Eurocurrency Rate and each Term SOFR Loan is due and payable on the last day of each interest period applicable thereto, and if such interest period extends over three months, at the end of each three-month interval during such interest period.

18

Table of Contents

The Amended Fourth A&R Credit Agreement is collateralized by substantially all of our assets. The Amended Fourth A&R Credit Agreement contains affirmative and negative covenants, representations and warranties, events of default and other terms customary for loans of this nature. In particular, the Amended Fourth A&R Credit Agreement requires that we maintain certain financial covenants, as follows:

 

Covenant Requirement

Consolidated Total Net Leverage Ratio (1)

 

5.0 to 1.0

Consolidated Senior Secured Net Leverage Ratio (2)

3.0 to 1.0

Consolidated Interest Coverage Ratio (3)

 

3.0 to 1.0

(1)Maximum Consolidated Total Net Leverage Ratio (as defined in the Amended Fourth A&R Credit Agreement) as of any fiscal quarter end.
(2)Maximum Consolidated Senior Secured Net Leverage Ratio (as defined in the Amended Fourth A&R Credit Agreement) as of any fiscal quarter end.
(3)Minimum ratio of Consolidated EBITDA (as defined in the Amended Fourth A&R Credit Agreement and adjusted for certain expenditures) to Consolidated Interest Expense (as defined in the Amended Fourth A&R Credit Agreement) for any period of four consecutive fiscal quarters.

We were in compliance with these financial covenants set forth in the Amended Fourth A&R Credit Agreement as of June 30, 2025.

As of June 30, 2025, we had no outstanding borrowings and issued letter of credit guarantees of $2.9 million under the Amended Fourth A&R Credit Agreement, with additional available borrowings of approximately $697 million, based on the maximum net leverage ratio required pursuant to the Amended Fourth A&R Credit Agreement.

Convertible Notes

In December 2023, we issued convertible notes which bear interest at 3.00% per year, payable semi-annually in arrears on February 1 and August 1 of each year, which commenced August 1, 2024 (the “Convertible Notes”). The Convertible Notes are senior unsecured obligations (as defined in the indenture governing the Convertible Notes (the “Indenture”)) of Merit and will mature on February 1, 2029, unless repurchased, redeemed or converted in accordance with their terms prior to such date. The net proceeds from the sale of the Convertible Notes were approximately $724.8 million after deducting offering and issuance costs and before the costs of the Capped Call Transactions, as described below.

The initial conversion rate of the notes will be 11.5171 shares of our common stock (the “Common Stock”) per $1,000 principal amount of notes, which equates to an initial conversion price of approximately $86.83 per share of Common Stock, subject to adjustments as provided in the Indenture upon the occurrence of certain specified events.

Conversion can occur at the option of the holders of the Convertible Notes (“Holders”) at any time on or after October 1, 2028. Prior to October 1, 2028, Holders may only elect to convert the Convertible Notes under the following circumstances: (1) During the five business day period after any ten consecutive trading day period in which, for each day of that period, the trading price per $1,000 principal amount of the Convertible Notes for such trading day was less than 98% of the product of the last reported sale price of the Common Stock and the applicable conversion rate on such trading day; (2) Merit issues to common shareholders any rights, options, or warrants, entitling them, for a period of not more than 60 days, to purchase shares of Common Stock at a price per share less than the average closing sale price of 10 consecutive trading days, or Merit’s election to make a distribution to common shareholders exceeding 10% of the previous day’s closing sale price; (3) Upon the occurrence of a Fundamental Change, as set forth in the Indenture; (4) During any calendar quarter (and only during such calendar quarter) beginning after March 31, 2024, if, the last reported sale price per share of the Common Stock exceeds 130% of the applicable conversion price on each applicable trading day for at least 20 trading days (whether or not consecutive) in the period of the 30 consecutive trading day period ending on, and including, the last trading day of the immediately preceding calendar quarter; or (5) Prior to the related redemption date if Merit calls any Convertible Notes for redemption. As of June 30, 2025, none of the conditions permitting the Holders to convert their Convertible Notes early had been met. Therefore, the Convertible Notes are classified as long-term debt obligations.

19

Table of Contents

Upon conversion, Merit will (1) pay cash up to the aggregate principal amount of the Convertible Notes to be converted and (2) pay or deliver, as the case may be, cash, shares of Common Stock, or a combination of cash and shares of Common Stock, at Merit’s election, in respect of the remainder, if any, of its conversion obligation in excess of the aggregate principal amount of the Convertible Notes being converted.

In addition, Holders will have the right to require Merit to repurchase all or a part of their notes upon the occurrence of a “fundamental change” (as defined in the Indenture) in cash at a fundamental change repurchase price of 100% of their principal amount plus accrued and unpaid interest up to, but excluding, the fundamental change repurchase date.

On or after February 7, 2027, we may redeem for cash all or part of the Convertible Notes, at our option, if the last reported sales price of Common Stock has been at least 130% of the conversion price then in effect for at least 20 trading days (whether or not consecutive), including the trading day immediately preceding the date on which we provide notice of redemption, during any 30 consecutive trading days ending on, and including, the trading day immediately before the date we send the related notice of the redemption.

Capped Call Transactions

In December 2023, in connection with the pricing of the Convertible Notes, Merit entered into privately negotiated capped call transactions (“Capped Call Transactions”) with certain of the initial purchasers and/or their respective affiliates and certain other financial institutions. The Capped Call Transactions cover, subject to customary anti-dilution adjustments, the number of shares of Common Stock initially underlying the Convertible Notes and are generally expected to reduce potential dilution to the Common Stock upon any conversion of Convertible Notes and/or offset any cash payments Merit is required to make in excess of the principal amount of converted Convertible Notes, as the case may be, with such reduction and/or offset subject to a cap, based on a cap price initially equal to approximately $114.68 per share of Common Stock, subject to certain adjustments under the terms of the Capped Call Transactions. The cost of the Capped Call Transactions was approximately $66.5 million. The Capped Call Transactions do not meet the criteria for separate accounting as a derivative as they are indexed to the Common Stock. The premiums paid for the Capped Call Transactions have been included as a net reduction to Common Stock within stockholders' equity.

20

Table of Contents

9.   Derivatives.

General. Our earnings and cash flows are subject to fluctuations due to changes in interest rates and foreign currency exchange rates, and we seek to mitigate a portion of the risks attributable to those fluctuations by entering into derivative contracts. The derivative instruments we use are interest rate swaps and foreign currency forward contracts. We recognize derivative instruments as either assets or liabilities at fair value in the accompanying consolidated balance sheets, regardless of whether hedge accounting is applied. We report cash flows arising from our hedging instruments consistent with the classification of cash flows from the underlying hedged items. Accordingly, cash flows associated with our derivative contracts are classified as operating activities in the accompanying consolidated statements of cash flows.

We formally document, designate and assess the effectiveness of transactions that receive hedge accounting treatment initially and on an ongoing basis. For qualifying hedges, the change in fair value is deferred in accumulated other comprehensive income, a component of stockholders’ equity in the accompanying consolidated balance sheets, and recognized in earnings at the same time the hedged item affects earnings. Changes in the fair value of derivative instruments not designated as hedging instruments are recorded in earnings throughout the term of the derivative.

Derivatives Designated as Cash Flow Hedges

In December 2019, we entered into a pay-fixed, receive-variable interest rate swap with a notional amount of $75 million with Wells Fargo wherein we fixed the one-month SOFR rate on that portion of our borrowings under the Amended Fourth A&R Credit Agreement. The term of the interest rate swap expired on July 31, 2024.

Foreign Currency Risk. We operate on a global basis and are exposed to the risk that our financial condition, results of operations, and cash flows could be adversely affected by changes in foreign currency exchange rates. To reduce the potential effects of foreign currency exchange rate movements on net earnings, we enter into derivative financial instruments in the form of foreign currency exchange forward contracts with major financial institutions. Our policy is to enter into foreign currency derivative contracts with maturities of up to two years. We are exposed to foreign currency exchange rate risk with respect to transactions and balances denominated in various currencies, with our most significant exposure related to transactions and balances denominated in Chinese Renminbi and Euros, among others. We do not use derivative financial instruments for trading or speculative purposes. We do not believe we are subject to any credit risk contingent features related to our derivative contracts, and we seek to manage counterparty risk by allocating derivative contracts among several major financial institutions.

Derivatives Designated as Cash Flow Hedges

For derivative instruments that are designated and qualify as cash flow hedges, the gain or loss on the derivative instrument is temporarily reported as a component of other comprehensive income and then reclassified into earnings in the same line item associated with the forecasted transaction and in the same period or periods during which the hedged transaction affects earnings. We entered into forward contracts on various foreign currencies to manage the risk associated with forecasted exchange rates which impact revenues, cost of sales, and operating expenses in various international markets. The objective of the forward contracts is to reduce the variability of cash flows associated with the forecasted purchase or sale of the foreign currencies. As of June 30, 2025 and December 31, 2024, we had entered into foreign currency forward contracts, which qualified as cash flow hedges, with aggregate notional amounts of $168.9 million and $117.5 million, respectively.

Derivatives Not Designated as Cash Flow Hedges

We forecast our net exposure in various receivables and payables to fluctuations in the value of various currencies, and we enter into foreign currency forward contracts to mitigate a portion of that exposure. As of June 30, 2025 and December 31, 2024, we had entered into foreign currency forward contracts related to those balance sheet accounts with aggregate notional amounts of $114.5 million and $95.7 million, respectively.

21

Table of Contents

Balance Sheet Presentation of Derivative Instruments. As of June 30, 2025 and December 31, 2024, all derivative instruments, both those designated as hedging instruments and those that were not designated as hedging instruments, were recorded at fair value on a gross basis on our consolidated balance sheets. We are not subject to any master netting agreements.

The fair value of derivative instruments on a gross basis was as follows on the dates indicated (in thousands):

Fair Value of Derivative Instruments Designated as Hedging Instruments

 

Balance Sheet Location

    

June 30, 2025

    

December 31, 2024

Assets

 

  

 

  

 

  

Foreign currency forward contracts

 

Prepaid expenses and other assets

$

2,439

$

3,771

Foreign currency forward contracts

 

Other assets (long-term)

899

 

1,064

(Liabilities)

 

  

 

  

 

  

Foreign currency forward contracts

 

Accrued expenses

 

(2,968)

 

(1,332)

Foreign currency forward contracts

 

Other long-term obligations

 

(1,167)

 

(287)

Fair Value of Derivative Instruments Not Designated as Hedging Instruments

 

Balance Sheet Location

    

June 30, 2025

    

December 31, 2024

Assets

 

  

 

  

 

  

Foreign currency forward contracts

 

Prepaid expenses and other assets

$

1,933

$

2,595

(Liabilities)

 

  

 

  

 

  

Foreign currency forward contracts

 

Accrued expenses

 

(1,153)

 

(1,288)

Income Statement Presentation of Derivative Instruments.

Derivative Instruments Designated as Cash Flow Hedges

Derivative instruments designated as cash flow hedges had the following effects, before income taxes, on other comprehensive income (“OCI”), accumulated other comprehensive income (“AOCI”), and net earnings in our consolidated statements of income, consolidated statements of comprehensive income and consolidated balance sheets (in thousands):

Amount of Gain/(Loss)

Consolidated Statements

Amount of Gain/(Loss)

Recognized in OCI

of Income

Reclassified from AOCI

Three Months Ended June 30, 

 

  

Three Months Ended June 30, 

Three Months Ended June 30, 

Derivative instrument

    

2025

 

2024

    

Location in statements of income

    

2025

  

  

2024

  

2025

  

  

2024

Interest rate swap

$

$

(197)

Interest expense

$

(6,775)

$

(7,679)

$

$

699

Foreign currency forward contracts

 

(1,396)

 

(31)

Revenue

 

382,462

 

338,003

 

509

 

427

Cost of sales

 

(197,975)

 

(176,903)

 

(242)

 

357

Amount of Gain/(Loss)

Consolidated Statements

Amount of Gain/(Loss)

Recognized in OCI

of Income

Reclassified from AOCI

Six Months Ended June 30, 

 

  

Six Months Ended June 30, 

Six Months Ended June 30, 

Derivative instrument

    

2025

 

2024

    

Location in statements of income

    

2025

 

2024

  

2025

 

 

2024

Interest rate swap

$

$

151

Interest expense

$

(13,343)

$

(15,725)

$

$

1,401

Foreign currency forward contracts

 

(3,293)

 

4,135

Revenue

 

737,813

 

661,511

 

1,530

 

840

Cost of sales

 

(381,306)

 

(348,696)

 

(774)

 

784

As of June 30, 2025, $0.2 million, or $0.2 million after taxes, was expected to be reclassified from AOCI to earnings in revenue and cost of sales over the succeeding twelve months.

22

Table of Contents

Derivative Instruments Not Designated as Hedging Instruments

The following gains/(losses) from these derivative instruments were recognized in our consolidated statements of income for the periods presented (in thousands):

    

    

Three Months Ended June 30, 

    

Six Months Ended June 30, 

Derivative Instrument

 

Location in statements of income

 

2025

 

2024

 

2025

 

2024

Foreign currency forward contracts

 

Other income (expense) — net

$

1,340

$

645

$

1,182

$

1,528

10.   Commitments and Contingencies.

Litigation. In the ordinary course of business, we are involved in various claims and litigation matters. These proceedings, actions and claims may involve product liability, intellectual property, contract disputes, employment, governmental inquiries or other matters, including the matter described below. These matters generally involve inherent uncertainties and often require prolonged periods of time to resolve. In certain proceedings, the claimants may seek damages as well as other compensatory and equitable relief that could result in the payment of significant claims and settlements and/or the imposition of injunctions or other equitable relief. For legal matters for which our management had sufficient information to reasonably estimate our future obligations, a liability representing management’s best estimate of the probable loss, or the minimum of the range of probable losses when a best estimate within the range is not known, is recorded. The estimates are based on consultation with legal counsel, previous settlement experience and settlement strategies. If actual outcomes are less favorable than those estimated by management, additional expense may be incurred, which could unfavorably affect our financial position, results of operations and cash flows. The ultimate cost to us with respect to actions and claims could be materially different than the amount of the current estimates and accruals and could have a material adverse effect on our financial position, results of operations and cash flows. Unless included in our legal accrual, we are unable to estimate a reasonably possible loss or range of loss associated with any individual material legal proceeding. Legal costs for these matters, such as outside counsel fees and expenses, are charged to expense in the period incurred.

SEC Inquiry

Commencing in January 2022, we have received requests from the Division of Enforcement of the U.S. Securities and Exchange Commission (“SEC”) seeking the voluntary production of information relating to the business activities of Merit’s subsidiary in China, including interactions with hospitals and health care officials in China (the “SEC Inquiry”). We are cooperating with the requests, investigating the matter and are engaged in steps in furtherance of reaching a resolution to the matter. Currently, we are unable to predict the scope, timing, significance or outcome of the SEC Inquiry or estimate a reasonably possible loss or range of loss associated with the matter. It is possible that the ultimate resolution of the SEC Inquiry, if resolved in a manner unfavorable to us, may be materially adverse to our business, financial position, results of operations or liquidity.

In management's opinion, based on its examination of these matters, its experience to date and discussions with counsel, other than the SEC Inquiry, we are not currently involved in any legal proceedings which, individually or in the aggregate, could have a material adverse effect on our financial position, results of operations or cash flows. Our management regularly assesses the risks of legal proceedings in which we are involved, and management’s view of these matters may change in the future.

23

Table of Contents

11.   Earnings Per Common Share (EPS). The computation of weighted average shares outstanding and the basic and diluted earnings per common share for the three and six-month periods ended June 30, 2025 and 2024 consisted of the following (in thousands, except per share amounts):

Three Months Ended

Six Months Ended

June 30, 

June 30, 

2025

2024

2025

2024

Net income

$

32,581

$

35,726

$

62,728

$

63,966

Average common shares outstanding

 

59,140

 

58,139

 

59,019

 

58,049

Basic EPS

$

0.55

$

0.61

$

1.06

$

1.10

Average common shares outstanding

59,140

58,139

59,019

58,049

Effect of dilutive stock awards

751

601

884

604

Effect of dilutive convertible notes

720

1,042

Total potential shares outstanding

60,611

58,740

60,945

58,653

Diluted EPS

$

0.54

$

0.61

$

1.03

$

1.09

Equity awards excluded as the impact was anti-dilutive (1)

245

802

165

1,009

(1)Does not reflect the impact of incremental repurchases under the treasury stock method.

Convertible Notes

For our Convertible Notes, the dilutive effect has been calculated using the if-converted method. Upon surrender of the Convertible Notes for conversion, Merit will pay cash up to the aggregate principal amount of the Notes to be converted and pay or deliver, as the case may be, cash, shares of Common Stock or a combination of cash and shares of Common Stock, at Merit’s election, in respect of the remainder, if any, of Merit’s conversion obligation in excess of the aggregate principal amount of the Convertible Notes being converted. Under the if-converted method, we include the number of shares required to satisfy the remaining conversion obligation, assuming all the Convertible Notes were converted. The convertible notes only have an impact on diluted earnings per share when the average share price of our Common Stock exceeds the conversion price of $86.83. The average closing price of the Common Stock for the three and six-month periods ended June 30, 2025 and 2024, respectively, was used as the basis for determining the dilutive effect on EPS.

24

Table of Contents

12.   Stock-Based Compensation Expense. Stock-based compensation expense before income tax expense for the three and six-month periods ended June 30, 2025 and 2024 consisted of the following (in thousands):

Three Months Ended

Six Months Ended

June 30, 

June 30, 

    

2025

    

2024

    

2025

    

2024

Cost of sales

Nonqualified stock options

$

305

$

363

$

651

$

725

Restricted stock units

340

622

Total cost of sales

645

363

1,273

725

Research and development

 

 

Nonqualified stock options

311

 

345

637

 

781

Restricted stock units

374

717

Total research and development

685

345

1,354

781

Selling, general and administrative

 

 

Nonqualified stock options

1,296

 

1,565

2,579

 

3,247

Performance-based restricted stock units

4,977

2,897

8,558

4,764

Restricted stock units

2,265

1,131

3,989

1,718

Cash-settled performance-based awards

903

710

2,096

1,010

Cash-settled restricted stock units

102

102

Total selling, general and administrative

9,543

6,303

17,324

10,739

Stock-based compensation expense before taxes

$

10,873

$

7,011

$

19,951

$

12,245

We recognize stock-based compensation expense (net of a forfeiture rate), for those awards which are expected to vest, on a straight-line basis over the requisite service period. We estimate the forfeiture rate based on our historical experience and expectations about future forfeitures.

Nonqualified Stock Options

During the six months ended June 30, 2025 and 2024, we did not grant any stock options. As of June 30, 2025, the total remaining unrecognized compensation cost related to non-vested stock options was $7.0 million, which was expected to be recognized over a weighted average period of 1.2 years.

Stock-Settled Performance-Based Restricted Stock Units (“Performance Stock Units”)

During the six-month periods ended June 30, 2025 and 2024, we granted Performance Stock Units which represented awards of up to 290,120 and 364,810 shares of Common Stock, respectively. Settlement of the Performance Stock Units into shares of Common Stock occurs at the end of the relevant performance periods. The actual number of shares of Common Stock issuable at the end of the performance periods is based upon Company performance towards specified financial performance targets and relative total shareholder return as compared to the Russell 2000 Index (“rTSR”), all as more specifically set forth in the Performance Stock Unit award agreements.

We use Monte-Carlo simulations to estimate the grant-date fair value of the Performance Stock Units linked to total shareholder return. The fair value of each performance stock unit was estimated as of the grant date using the following assumptions for awards granted in the periods indicated below:

Six Months Ended

June 30, 

2025

2024

Risk-free interest rate

    

4.0%

  

4.4%

Performance period

 

2.8 years

 

2.8 years

Expected dividend yield

 

 

Expected price volatility

 

28.0%

  

31.1%

25

Table of Contents

The risk-free interest rate of return was determined using the U.S. Treasury rate at the time of grant with a term equal to the expected term of the award. The expected volatility was based on the weighted average volatility of our stock price and the average volatility of our compensation peer group's stock price. The expected dividend yield was assumed to be zero because, at the time of the grant, we had no plans to declare a dividend.

Compensation expense is recognized using the grant-date fair value for the number of shares that are likely to be awarded based on the performance metrics. Each reporting period, this probability assessment is updated, and cumulative adjustments are recorded based on the financial performance metrics expected to be achieved. At the end of the performance period, cumulative expense is calculated based on the actual performance metrics achieved. As of June 30, 2025, the total remaining unrecognized compensation cost related to stock-settled Performance Stock Units was $33.8 million, which is expected to be recognized over a weighted average period of 1.5 years.

Cash-Settled Performance-Based Awards

During the six-month periods ended June 30, 2025 and 2024, we granted Performance Stock Units to our Chief Executive Officer that provide for settlement in cash upon achievement of specific metrics (“Liability Awards”), with total target cash incentives in the amount of $1.7 million and $1.6 million, respectively. The Liability Awards entitle him to a target cash payment based upon our level of rTSR performance and achievement of other performance metrics, as defined in the award agreements.

During the six-month periods ended June 30, 2025 and 2024, we granted additional Performance Stock Units to certain employees that provide for settlement in cash upon our achievement of specified financial metrics. The cash payable upon vesting at the end of the service period is based upon performance against specified financial performance targets and relative total shareholder return as compared to the rTSR, as defined in the award agreements. Compensation expense is recognized in an amount equal to the cash payment likely to be awarded based on the performance metrics.

The potential maximum payout of these Liability Awards is 250% of the target cash incentive, resulting in a total potential maximum payout of $4.7 million and $4.4 million for Liability Awards granted during the six-month periods ended June 30, 2025 and 2024, respectively. The settlement generally occurs at the end of three-year performance periods based upon the same performance metrics and vesting period as our Performance Stock Units.

The fair value of these Liability Awards is measured at each reporting period until the awards are settled. As of June 30, 2025 and December 31, 2024, the recorded balance associated with these Liability Awards was $4.7 million and $5.1 million, respectively, which have been classified as liabilities and reported in accrued expenses and other long-term obligations within our consolidated balance sheets. As of June 30, 2025, the total remaining unrecognized compensation cost related to Liability Awards was $5.7 million, which was expected to be recognized over a weighted average period of 1.6 years.

Restricted Stock Units

During the six-month periods ended June 30, 2025 and 2024, we granted restricted stock units to certain employees and non-employee directors representing 135,778 and 158,719 shares of Common Stock, respectively. The expense recognized for restricted stock units is equal to the closing stock price on the date of grant, which is recognized over the vesting period. Restricted stock units granted to each employee are subject to such employee’s continued employment through the vesting date, which is four years from the date of grant. Restricted stock units granted to each non-employee director are subject to such director’s continued service through the vesting date, which is one year from the grant date. As of June 30, 2025, the total remaining unrecognized compensation cost related to restricted stock units was $30.8 million, which was expected to be recognized over a weighted average period of 2.9 years.

26

Table of Contents

13.   Segment Reporting. We report our operations in two operating segments: cardiovascular and endoscopy. Our cardiovascular segment consists of four product categories: peripheral intervention, cardiac intervention, custom procedural solutions, and OEM. Within these product categories, we sell a variety of products, including cardiology and radiology devices (which assist in diagnosing and treating coronary arterial disease, peripheral vascular disease and other non-vascular diseases), as well as embolotherapeutic, cardiac rhythm management, electrophysiology, critical care, breast cancer localization and guidance, biopsy, and interventional oncology and spine devices. Our endoscopy segment consists of gastroenterology and pulmonology devices which assist in the palliative treatment of expanding esophageal, tracheobronchial and biliary strictures. Our chief operating decision maker (“CODM”) is our Chief Executive Officer, who uses segment profit or loss to assess performance and allocate resources to each segment, primarily through periodic budgeting and segment performance reviews. See Note 3, Revenues from Contracts with Customers for a detailed breakout of our sales by operating segment and product category, disaggregated between domestic and international sales. Total assets by segment are not used by the CODM to assess performance or allocate resources to the Company’s segments; therefore, total assets by segment are not disclosed.

Financial information relating to our reportable operating segments and reconciliations to the consolidated totals for the three and six-month periods ended June 30, 2025 and 2024, were as follows (in thousands):

Three Months Ended

Three Months Ended

June 30, 2025

June 30, 2024

  

Cardiovascular

  

Endoscopy

  

Consolidated

  

Cardiovascular

  

Endoscopy

  

Consolidated

Net sales

 

$

364,025

 

$

18,437

 

$

382,462

 

$

327,815

$

10,188

 

$

338,003

Cost of sales standard(1)

147,710

4,342

140,492

3,256

Cost of sales other(2)

 

43,949

 

1,974

 

 

32,828

 

327

 

Selling, general and administrative expenses

 

107,673

 

5,424

 

 

91,634

 

2,951

 

Research and development expenses

23,306

1,061

19,643

620

Other operating expenses(3)

143

306

Income from operations

$

41,244

$

5,636

$

46,880

$

42,912

$

3,034

$

45,946

Total other expense — net

(3,501)

(103)

 

  

 

  

 

  

 

  

 

  

 

  

Income before income taxes

 

$

43,379

 

$

45,843

Six Months Ended

Six Months Ended

June 30, 2025

June 30, 2024

  

Cardiovascular

  

Endoscopy

  

Consolidated

  

Cardiovascular

  

Endoscopy

  

Consolidated

Net sales

 

$

702,738

 

$

35,075

 

$

737,813

 

$

641,189

$

20,322

 

$

661,511

Cost of sales standard(1)

286,151

8,705

273,558

6,365

Cost of sales other(2)

 

81,732

 

4,718

 

 

68,130

 

643

 

Selling, general and administrative expenses

 

208,647

 

11,936

 

 

182,934

 

6,079

 

Research and development expenses

45,260

1,585

40,559

1,186

Other operating expenses(3)

1,166

189

Income from operations

$

79,782

$

8,131

$

87,913

$

75,819

$

6,049

$

81,868

Total other expense — net

(6,576)

(1,677)

 

  

 

  

 

  

 

  

 

  

 

  

Income before income taxes

 

$

81,337

 

$

80,191

(1)Cost of sales standard represents costs of goods sold measured at the internal standard cost for production of inventory. Inventory standard costs include material, labor and manufacturing overhead.
(2)Cost of sales other for all segments includes amortization expense associated with our developed technology and license agreement intangible assets, freight and handling associated with shipments to customers, provisions based on estimated excess, slow moving and obsolete inventories, manufacturing and price variances, and royalties.
(3)Other operating expenses include contingent consideration expense (benefit) related to the changes in fair value of contingent payments associated with acquisitions.

27

Table of Contents

Total depreciation and amortization by operating segment for the three and six-month periods ended June 30, 2025 and 2024, consisted of the following (in thousands):

Three Months Ended

Six Months Ended

June 30, 

June 30, 

2025

2024

2025

2024

Cardiovascular

$

28,767

$

23,964

$

55,737

$

47,352

Endoscopy

2,254

127

4,576

338

Total

$

31,021

$

24,091

$

60,313

$

47,690

14.   Fair Value Measurements.

Assets (Liabilities) Measured at Fair Value on a Recurring Basis

Our financial assets and (liabilities) carried at fair value and measured on a recurring basis as of June 30, 2025 and December 31, 2024 consisted of the following (in thousands):

Fair Value Measurements Using

Total Fair

Quoted prices in

Significant other

Significant

Value at

active markets

observable inputs

unobservable inputs

    

June 30, 2025

    

(Level 1)

    

(Level 2)

    

(Level 3)

Money market funds (1)

$

30,652

$

30,652

$

United States treasury debt securities (2)

$

7,718

$

7,718

$

Foreign currency contract assets, current and long-term (3)

$

5,271

$

$

5,271

$

Foreign currency contract liabilities, current and long-term (4)

$

(5,288)

$

$

(5,288)

$

Contingent consideration liabilities

$

(2,027)

$

$

$

(2,027)

Fair Value Measurements Using

Total Fair

Quoted prices in

Significant other

Significant

Value at

active markets

observable inputs

unobservable inputs

    

December 31, 2024

    

(Level 1)

    

(Level 2)

    

(Level 3)

Money market funds (1)

$

10,034

$

10,034

$

Marketable securities (5)

$

92

$

92

$

Foreign currency contract assets, current and long-term (3)

$

7,430

$

$

7,430

$

Foreign currency contract liabilities, current and long-term (4)

$

(2,907)

$

$

(2,907)

$

Contingent consideration liabilities

$

(3,486)

$

$

$

(3,486)

(1)Our money market fund represents a bank-managed money market fund which permits daily redemptions. Amounts in the fund are recorded as cash equivalents in the consolidated balance sheets.
(2)The fair value of U.S. treasury debt securities are determined using quoted prices for identical assets in active markets and is recorded as cash and cash equivalents in the consolidated balance sheets.
(3)The fair value of the foreign currency contract assets (including those designated as hedging instruments and those not designated as hedging instruments) is determined using Level 2 fair value inputs and is recorded as a prepaid expense and other current asset or other long-term asset in the consolidated balance sheets.
(4)The fair value of the foreign currency contract liabilities (including those designated as hedging instruments and those not designated as hedging instruments) is determined using Level 2 fair value inputs and is recorded as accrued expense or other long-term obligation in the consolidated balance sheets.
(5)Our marketable securities, which consist entirely of available-for-sale equity securities, are valued using market prices in active markets. Level 1 instrument valuations are obtained from real-time quotes for transactions in active exchange markets involving identical assets.

28

Table of Contents

Certain of our past business combinations involve the potential for the payment of future contingent consideration, generally based on a percentage of future product sales or upon attaining specified future revenue or other milestones. The contingent consideration liability is re-measured at the estimated fair value at the end of each reporting period with the change in fair value recognized within operating expenses in the accompanying consolidated statements of income for such period. We measure the initial liability and re-measure the liability on a recurring basis using Level 3 inputs as defined under authoritative guidance for fair value measurements. Changes in the fair value of our contingent consideration liabilities during the three and six-month periods ended June 30, 2025 and 2024 consisted of the following (in thousands):

    

Three Months Ended

    

Six Months Ended

    

June 30, 

    

June 30, 

    

2025

    

2024

    

2025

    

2024

Beginning balance

$

4,429

$

3,225

$

3,486

$

3,447

Contingent consideration expense

 

143

 

305

 

1,166

 

188

Contingent payments made

 

(2,545)

 

(95)

 

(2,625)

 

(200)

Ending balance

$

2,027

$

3,435

$

2,027

$

3,435

As of June 30, 2025, $1.7 million in contingent consideration liability was included in other long-term obligations and $0.3 million in contingent consideration liability was included in accrued expenses in our consolidated balance sheet. As of December 31, 2024, $3.1 million in contingent consideration liability was included in other long-term obligations and $0.4 million in contingent consideration liability was included in accrued expenses in our consolidated balance sheet.

Payments related to the settlement of the contingent consideration liability recognized at fair value as of the applicable acquisition date of $2.5 million and $0.1 million for the six-month periods ended June 30, 2025 and 2024, respectively, have been reflected as a cash outflow from financing activities in the accompanying consolidated statements of cash flows. Payments related to increases in the contingent consideration liability subsequent to the date of acquisition of $0.1 million and $0.1 million for the six-month periods ended June 30, 2025 and 2024, respectively, are reflected as operating cash flows.

29

Table of Contents

The recurring Level 3 measurement of our contingent consideration liabilities included the following significant unobservable inputs at June 30, 2025 and December 31, 2024 (amounts in thousands):

Fair value at

    

June 30, 

Valuation

Weighted

Contingent consideration liability

    

2025

    

technique

    

Unobservable inputs

    

Range

Average(1)

Revenue-based royalty payments contingent liability

$

1,936

 

Discounted cash flow

 

Discount rate

13.0% - 15.0%

13.5%

 

  

 

 

Projected year of payments

2025-2034

2029

Revenue milestones contingent liability

$

91

 

Monte Carlo simulation

 

Discount rate

11.0%

 

  

 

 

Projected year of payments

2025-2041

2041

Fair value at

    

December 31, 

Valuation

Weighted

Contingent consideration liability

    

2024

    

technique

    

Unobservable inputs

    

Range

Average(1)

Revenue-based royalty payments contingent liability

$

2,217

 

Discounted cash flow

 

Discount rate

14.0% - 16.0%

14.6%

 

  

 

 

Projected year of payments

2025-2034

2028

Revenue milestones contingent liability

$

88

 

Monte Carlo simulation

 

Discount rate

13.0%

 

  

 

 

Projected year of payments

2025-2040

2039

Regulatory approval contingent liability

$

1,181

Scenario-based method

Discount rate

6.0%

Probability of milestone payment

50.0%

Projected year of payment

2025-2026

2025

(1)Unobservable inputs were weighted by the relative fair value of the instruments. No weighted average is reported for contingent consideration liabilities without a range of unobservable inputs.

The contingent consideration liability is re-measured to fair value each reporting period. Significant increases or decreases in projected revenues, based on our most recent internal operational budgets and long-range strategic plans, discount rates or the time until payment is made would have resulted in a significantly lower or higher fair value measurement. Our determination of the fair value of the contingent consideration liability could change in future periods based upon our ongoing evaluation of these significant unobservable inputs. We intend to record any such change in the fair value of contingent consideration liability to operating expenses in our consolidated statements of income.

Fair Value of Other Assets (Liabilities)

The carrying amount of cash and cash equivalents, receivables, and trade payables approximate fair value because of the immediate, short-term maturity of these financial instruments. The fair value of our long-term debt under our Convertible Notes was $934.4 million as of June 30, 2025 and was determined based on quoted prices in markets that are not active, which is considered a Level 2 valuation input. The fair value of assets and liabilities whose carrying value approximates fair value is determined using Level 2 inputs, with the exception of cash and cash equivalents, which use Level 1 inputs.

We recognize or disclose the fair value of certain assets, such as non-financial assets, primarily property and equipment, right-of-use operating lease assets, equity investments, intangible assets and goodwill in connection with impairment evaluations. Such assets are reported at carrying value and are not subject to recurring fair value measurements. We review our long-lived assets for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. Fair value is generally determined based on discounted future cash flow. All our nonrecurring valuations use significant unobservable inputs and therefore fall under Level 3 of the fair value hierarchy.

30

Table of Contents

Our equity investments in privately-held companies were $25.9 million and $22.8 million at June 30, 2025 and December 31, 2024, respectively, which are included within other long-term assets in our consolidated balance sheets. We analyze our investments in privately-held companies to determine if they should be accounted for using the equity method based on our ability to exercise significant influence over operating and financial policies of the investment whereby we record our proportionate share of the investee’s earnings or losses; amortization of differences between our investment basis and underlying equity in net assets of the investee, excluding the component representing goodwill; and impairment, if any, as a component of other income (expense) — net for each reporting period. Investments not accounted for under the equity method of accounting are accounted for at cost minus impairment, if applicable, plus or minus changes in valuation resulting from observable transactions for identical or similar investments. For the six-month periods ended June 30, 2025 and 2024, we recorded no impairment charges related to our equity investments.

Current Expected Credit Losses

Our outstanding long-term notes receivable, including accrued interest and an allowance for current expected credit losses, were $21.0 million and $9.4 million as of June 30, 2025 and December 31, 2024, respectively. Long-term notes receivable increased $11.6 million for the six-month period ended June 30, 2025 related to loans issued to FluidX Medical Technology, Inc. and Protaryx Medical Inc. As of June 30, 2025 and December 31, 2024, we had an allowance for current expected credit losses of $2.4 million and $1.4 million, respectively, associated with these notes receivable. We assess the allowance for current expected credit losses on an individual security basis, due to the limited number of securities, using a probability of default model, which is based on relevant information about past events, including historical experience, current conditions and reasonable and supportable forecasts that affect the expected collectability of securities, and other security specific factors.

The table below presents a roll-forward of the allowance for current expected credit losses on our notes receivable for the three and six-month periods ended June 30, 2025 and 2024 (in thousands):

Three Months Ended

Six Months Ended

June 30, 

June 30, 

2025

    

2024

2025

    

2024

Beginning balance

$

1,634

$

1,388

$

1,366

$

568

Provision for credit loss expense

741

18

1,009

838

Ending balance

$

2,375

$

1,406

$

2,375

$

1,406

31

Table of Contents

15. Accumulated Other Comprehensive Income (Loss). The changes in each component of accumulated other comprehensive income (loss) for the three and six-month periods ended June 30, 2025 and 2024 were as follows:

Cash Flow Hedges

    

Foreign Currency Translation

    

Total

Balance as of April 1, 2025

$

942

$

(16,318)

$

(15,376)

Other comprehensive income (loss)

 

(1,396)

13,200

11,804

Income taxes

 

393

(1,616)

(1,223)

Reclassifications to:

Revenue

(509)

(509)

Cost of sales

242

242

Net other comprehensive income (loss)

(1,270)

11,584

10,314

Balance as of June 30, 2025

$

(328)

$

(4,734)

$

(5,062)

Cash Flow Hedges

    

Foreign Currency Translation

    

Total

Balance as of April 1, 2024

$

3,932

$

(16,388)

$

(12,456)

Other comprehensive loss

 

(228)

(1,688)

(1,916)

Income taxes

 

404

22

426

Reclassifications to:

Revenue

(427)

(427)

Cost of sales

(357)

(357)

Interest expense

(699)

(699)

Net other comprehensive loss

(1,307)

(1,666)

(2,973)

Balance as of June 30, 2024

$

2,625

$

(18,054)

$

(15,429)

Cash Flow Hedges

    

Foreign Currency Translation

    

Total

Balance as of January 1, 2025

$

2,765

$

(22,166)

$

(19,401)

Other comprehensive income (loss)

 

(3,293)

19,054

15,761

Income taxes

 

956

(1,622)

(666)

Reclassifications to:

Revenue

(1,530)

(1,530)

Cost of sales

774

774

Net other comprehensive income (loss)

(3,093)

17,432

14,339

Balance as of June 30, 2025

$

(328)

$

(4,734)

$

(5,062)

Cash Flow Hedges

    

Foreign Currency Translation

    

Total

Balance as of January 1, 2024

$

1,662

$

(12,996)

$

(11,334)

Other comprehensive income (loss)

 

4,286

(5,092)

(806)

Income taxes

 

(298)

34

(264)

Reclassifications to:

Revenue

(840)

(840)

Cost of sales

(784)

(784)

Interest expense

(1,401)

(1,401)

Net other comprehensive income (loss)

963

(5,058)

(4,095)

Balance as of June 30, 2024

$

2,625

$

(18,054)

$

(15,429)

32

Table of Contents

ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

The following discussion and analysis of our financial condition and results of operations should be read in conjunction with the consolidated financial statements and related condensed notes thereto, which are included in Part I of this report. Our future financial condition and results of operations, as well as any forward-looking statements, are subject to inherent risks and uncertainties that may adversely impact our operations and financial results. These risks and uncertainties are discussed in Part I, Item 1A “Risk Factors” in the 2024 Annual Report on Form 10-K and in Part II, Item 1A “Risk Factors” in this report.

OVERVIEW

We are a leading manufacturer and marketer of proprietary medical devices used in interventional, diagnostic and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care and endoscopy. Our cardiovascular segment consists of four product categories: peripheral intervention, cardiac intervention, custom procedural solutions, and OEM. Within these product categories, we sell a variety of products, including cardiology and radiology devices (which assist in diagnosing and treating coronary arterial disease, peripheral vascular disease and other non-vascular diseases), as well as embolotherapeutic, cardiac rhythm management, electrophysiology, critical care, breast cancer localization and guidance, biopsy, and interventional oncology and spine devices. Our endoscopy segment consists of gastroenterology and pulmonology devices which assist in the palliative treatment of expanding esophageal, tracheobronchial and biliary strictures.

For the three-month period ended June 30, 2025, we reported sales of $382.5 million, an increase of $44.5 million or 13.2% compared to sales for the three-month period ended June 30, 2024 of $338.0 million. For the six-month period ended June 30, 2025, we reported sales of $737.8 million, an increase of $76.3 million or 11.5%% compared to sales for the six-month period ended June 30, 2024 of $661.5 million. Foreign currency fluctuations (net of hedging) increased/(decreased) our net sales by $2.3 million and $(1.1) million for the three and six-month periods ended June 30, 2025, respectively, assuming applicable foreign exchange rates in effect during the comparable prior-year periods.

Gross profit as a percentage of sales increased to 48.2% for the three-month period ended June 30, 2025 compared to 47.7% for the three-month period ended June 30, 2024. Gross profit as a percentage of sales increased to 48.3% for the six-month period ended June 30, 2025 compared to 47.3% for the six-month period ended June 30, 2024.

Net income for the three-month period ended June 30, 2025 was $32.6 million, or $0.54 per share, compared to net income of $35.7 million, or $0.61 per share, for the three-month period ended June 30, 2024. Net income for the six-month period ended June 30, 2025 was $62.7 million, or $1.03 per share, compared to net income of $64.0 million, or $1.09 per share, for six-month period ended June 30, 2024.

Recent Developments and Trends

In addition to the trends identified in the 2024 Annual Report on Form 10-K under the heading “Management’s Discussion and Analysis of Financial Condition and Results of Operations - Overview,” our business in 2025 has been impacted, and we believe will continue to be impacted, by the following recent developments and trends:

Our revenue results during the three-month period ended June 30, 2025 were driven primarily by demand in the U.S. and favorable international sales trends, particularly in our Rest of World (“ROW”) and Europe, the Middle East and Africa (“EMEA) regions.
As of June 30, 2025, we had cash, cash equivalents, and restricted cash of $343.9 million and net available borrowing capacity under our Fourth A&R Credit Agreement of approximately $697 million.

33

Table of Contents

The United States recently announced changes to its trade policies, including increasing tariffs on imports, in some cases significantly, and potentially negotiating or terminating existing trade agreements. These actions have prompted retaliatory tariffs and other measures by a number of countries. While the long-term effects remain uncertain, we continue to closely monitor the evolving trade policy environment which presents a mix of impacts, including, among other impacts, the potential for increased production costs and higher pricing to our customers, any of which could negatively affect our business, results of operations and financial condition. See Part II, Item 1A. Risk Factors in this report.

RESULTS OF OPERATIONS

The following table sets forth certain operational data as a percentage of sales for the periods indicated:

    

Three Months Ended

Six Months Ended

June 30, 

June 30, 

    

2025

    

2024

    

    

2025

    

2024

    

Net sales

 

100

%  

100

%  

 

100

%  

100

%  

Gross profit

 

48.2

 

47.7

 

 

48.3

47.3

 

Selling, general and administrative expenses

 

29.6

 

28.0

 

 

29.9

28.6

 

Research and development expenses

 

6.4

 

6.0

 

 

6.3

6.3

 

Contingent consideration expense

 

0.0

 

0.1

 

 

0.2

0.0

 

Income from operations

 

12.3

 

13.6

 

 

11.9

12.4

 

Other expense — net

 

(0.9)

 

(0.0)

 

 

(0.9)

(0.3)

 

Income before income taxes

 

11.3

 

13.6

 

 

11.0

12.1

 

Net income

 

8.5

 

10.6

 

 

8.5

9.7

 

Sales

Sales for the three-month period ended June 30, 2025 increased by 13.2%, or $44.5 million, compared to the corresponding period in 2024. Sales for six-month period ended June 30, 2025 increased by 11.5%, or $76.3 million, compared to the corresponding period in 2024. Listed below are the sales by product category within each of our reportable segments for the three and six-month periods ended June 30, 2025 and 2024 (in thousands, other than percentage changes):

    

Three Months Ended

Six Months Ended

    

June 30, 

June 30, 

    

% Change

    

2025

    

2024*

    

% Change

    

2025

    

2024*

Cardiovascular

Peripheral Intervention

 

6.3

%  

$

142,847

$

134,386

5.9

%  

$

280,126

$

264,452

Cardiac Intervention

 

23.5

%  

 

115,251

 

93,307

 

17.2

%  

214,992

 

183,483

Custom Procedural Solutions

 

7.0

%  

 

53,634

 

50,132

 

3.0

%  

101,576

 

98,655

OEM

 

4.6

%  

 

52,293

 

49,990

 

12.1

%  

106,044

 

94,599

Total

 

11.0

%  

 

364,025

 

327,815

 

9.6

%  

702,738

 

641,189

Endoscopy

Endoscopy Devices

 

81.0

%  

 

18,437

 

10,188

 

72.6

%  

35,075

 

20,322

Total

 

13.2

%  

$

382,462

$

338,003

11.5

%  

$

737,813

$

661,511

*Commencing January 1, 2025, we reorganized our sales teams and product categories to include revenues from the sale of our spine devices under our OEM product category. Revenue figures for 2024 have been recast to reflect this realignment of our portfolio of spine products, representing approximately $5.7 million and $11.0 million in revenue for the three and six-month periods ended June 30, 2024, within the OEM product category to provide comparability between the reported periods.

34

Table of Contents

Cardiovascular Sales. Our cardiovascular sales for the three-month period ended June 30, 2025 were $364.0 million, up 11.0% when compared to the corresponding period of 2024 of $327.8 million. Sales for the three-month period ended June 30, 2025 were favorably affected by increased sales of:

(a)Peripheral intervention products, which increased by $8.5 million, or 6.3%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our radar localization, drainage, embolotherapy and delivery systems products.
(b)Cardiac intervention products, which increased by $21.9 million, or 23.5%, from the corresponding period of 2024. This increase was driven primarily by $10.2 million in sales associated with products acquired from Cook in November 2024 and increased sales of our intervention and angiography products.
(c)OEM products, which increased by $2.3 million, or 4.6%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our cardiac rhythm management/electrophysiology (“CRM/EP”), kits and intervention products, offset partially by decreased sales of our access and coatings products.
(d)Custom procedural solutions products, which increased by $3.5 million, or 7.0%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our critical care products.

Our cardiovascular sales for the six-month period ended June 30, 2025 were $702.7 million, up 9.6% when compared to the corresponding period of 2024 of $641.2 million. Sales for the six-month period ended June 30, 2025 were favorably affected by increased sales of:

(a)Peripheral intervention products, which increased by $15.7 million, or 5.9%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our access, embolotherapy, radar localization, drainage and delivery systems products.
(b)Cardiac intervention products, which increased by $31.5 million, or 17.2%, from the corresponding period of 2024. This increase was driven primarily by $19.4 million in sales associated with products acquired from Cook in November 2024 and increased sales of our CRM/EP, intervention and fluid management products.
(c)OEM products, which increased by $11.4 million, or 12.1%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our kits, intervention and angiography products, offset partially by decreased sales of our fluid management and coatings products.
(d)Custom procedural solutions products, which increased by $2.9 million, or 3.0%, from the corresponding period of 2024. This increase was driven primarily by increased sales of our critical care and trays products.

Endoscopy Sales. Our endoscopy sales for the three-month period ended June 30, 2025 were $18.4 million, up 81.0% when compared to sales in the corresponding period of 2024 of $10.2 million. Sales for the three-month period ended June 30, 2025 compared to the corresponding period in 2024 were favorably affected by $8.1 million in sales of the EsophyX® Z+ device acquired from EGS in July 2024.

Our endoscopy sales for the six-month period ended June 30, 2025 were $35.1 million, up 72.6% when compared to sales in the corresponding period of 2024 of $20.3 million. Sales for the six-month period ended June 30, 2025 compared to the corresponding period in 2024 were favorably affected by $14.7 million in sales of the EsophyX® Z+ device acquired from EGS in July 2024.

35

Table of Contents

Geographic Sales

Listed below are sales by geography for the three and six-month periods ended June 30, 2025 and 2024 (in thousands, other than percentage changes):

    

Three Months Ended

Six Months Ended

    

June 30, 

June 30, 

    

% Change

    

2025

    

2024

    

% Change

    

2025

    

2024

United States

16.7

%

$

227,082

$

194,664

15.7

%  

$

440,646

$

380,758

International

8.4

%

155,380

143,339

5.8

%  

297,167

280,753

Total

 

13.2

%  

$

382,462

$

338,003

11.5

%  

$

737,813

$

661,511

United States Sales. U.S. sales for the three-month period ended June 30, 2025 were $227.1 million, or 59.4% of net sales, up 16.7% when compared to the corresponding period of 2024. The increase in our domestic sales for the three-month period ended June 30, 2025, compared to the corresponding period of 2024 was driven primarily by our U.S. Direct, OEM and Endoscopy businesses.

U.S. sales for the six-month period ended June 30, 2025 were $440.6 million, or 59.7%% of net sales, up 15.7% when compared to the corresponding period of 2024. The increase in our domestic sales for the six-month period ended June 30, 2025, compared to the corresponding period of 2024 was driven primarily by our U.S. Direct, OEM and Endoscopy businesses.

International Sales. International sales for the three-month period ended June 30, 2025 were $155.4 million, or 40.6% of net sales, up 8.4% when compared to the corresponding period of 2024 of $143.3 million. The increase in our international sales for the three-month period ended June 30, 2025, compared to the corresponding period of 2024 included increased sales in our ROW operations of $2.0 million or 14.0% and our EMEA operations of $10.3 million or 16.5%, partially offset by decreased sales in our Asia Pacific (“APAC”) operations of $(0.2) million or (0.4)%.

International sales for the six-month period ended June 30, 2025 were $297.2 million, or 40.3% of net sales, up 5.8% when compared to the corresponding period of 2024 of $280.8 million. The increase in our international sales for the six-month period ended June 30, 2025, compared to the corresponding period of 2024 included increased sales in our ROW operations of $4.4 million or 15.8% and our EMEA operations of $12.6 million or 10.2%, partially offset by decreased sales in our APAC operations of $(0.5) million or (0.4)%.

Gross Profit

Our gross profit as a percentage of sales increased to 48.2% for the three-month period ended June 30, 2025, compared to 47.7% for the three-month period ended June 30, 2024. The increase in gross profit percentage was primarily due to an increase in sales combined with favorable changes in product mix, partially offset by higher intangible amortization expense as a percentage of sales associated with acquisitions.

Our gross profit as a percentage of sales increased to 48.3% for the six-month period ended June 30, 2025, compared to 47.3% for the six-month period ended June 30, 2024. The increase in gross profit percentage was primarily due to an increase in sales combined with favorable changes in product mix, partially offset by higher intangible amortization expense as a percentage of sales associated with acquisitions.

36

Table of Contents

Operating Expenses

Selling, General and Administrative Expense. Selling, general and administrative ("SG&A") expenses increased $18.5 million, or 19.6%, for the three-month period ended June 30, 2025 compared to the corresponding period of 2024. As a percentage of sales, SG&A expenses were 29.6% for the three-month period ended June 30, 2025, compared to 28.0% for the corresponding period of 2024. SG&A expenses increased $31.6 million, or 16.7%, for the six-month period ended June 30, 2025 compared to the corresponding period of 2024. As a percentage of sales, SG&A expenses were 29.9%% for the six-month period ended June 30, 2025, compared to 28.6%% for the corresponding period of 2024. For the three and six-month periods ended June 30, 2025, SG&A expenses increased compared to the corresponding periods of 2024, primarily due to an increase in labor-related costs associated with headcount additions, including those in connection with the EGS, Cook and Biolife Acquisitions, and increased travel and entertainment and advertising and promotional expenses.

Research and Development Expenses. Research and development (”R&D”) expenses for the three-month period ended June 30, 2025 were $24.4 million, up 20.3%, when compared to R&D expenses in the corresponding period of 2024 of $20.3 million. R&D expenses for the six-month period ended June 30, 2025 were $46.8 million, up 12.2%, when compared to R&D expenses in the corresponding period of 2024 of $41.7 million. For the three and six-month periods ended June 30, 2025, R&D expenses increased compared to the corresponding periods of 2024 primarily due to increased R&D activity and regulatory costs associated with clinical trials.

Contingent Consideration Expense. For the three and six-month periods ended June 30, 2025, we recognized contingent consideration expense from changes in the estimated fair value of our contingent consideration obligations stemming from our previously disclosed business acquisitions of $0.1 million and $1.2 million, compared to contingent consideration expense of $0.3 million and $0.2 million for the three and six-month periods ended June 30, 2024. Expense in each period related to changes in the probability and timing of achieving certain revenue and operational milestones, as well as expense for the passage of time.

Operating Income

The following table sets forth our operating income by financial reporting segment for the three and six-month periods ended June 30, 2025 and 2024 (in thousands):

Three Months Ended

Six Months Ended

June 30, 

June 30, 

    

2025

    

2024

    

2025

    

2024

Operating Income

Cardiovascular

$

41,244

$

42,912

$

79,782

$

75,819

Endoscopy

 

5,636

 

3,034

 

8,131

 

6,049

Total operating income

$

46,880

$

45,946

$

87,913

$

81,868

Cardiovascular Operating Income. Our cardiovascular operating income for the three-month period ended June 30, 2025 was $41.2 million, compared to cardiovascular operating income in the corresponding period of 2024 of $42.9 million. The decrease in cardiovascular operating income during the three-month period ended June 30, 2025 compared to the corresponding period of 2024 was primarily a result of increased SG&A and R&D expense, partially offset by increased sales ($364.0 million compared to $327.8 million) and gross margin.

Our cardiovascular operating income for the six-month period ended June 30, 2025 was $79.8 million, compared to cardiovascular operating income in the corresponding period of 2024 of $75.8 million. The increase in cardiovascular operating income during the six-month period ended June 30, 2025 compared to the corresponding period of 2024 was primarily a result of increased sales ($702.7 million compared to $641.2 million) and gross margin, partially offset by increased SG&A, R&D and contingent consideration expenses.

37

Table of Contents

Endoscopy Operating Income. Our endoscopy operating income for the three-month period ended June 30, 2025 was $5.6 million, compared to endoscopy operating income of $3.0 million for the corresponding period of 2024. Our endoscopy operating income for the six-month period ended June 30, 2025 was $8.1 million, compared to endoscopy operating income of $6.0 million for the corresponding period of 2024. The increase in endoscopy operating income for the three and six-month periods ended June 30, 2025 compared to the corresponding periods of 2024 was primarily a result of increased sales and gross margin, partially offset by increased SG&A expenses associated with higher labor related costs due to headcount additions in connection with the integration activities for the EGS Acquisition.

Other Expense – Net

Our other expense for the three months ended June 30, 2025 and 2024 was $3.5 million and $0.1 million, respectively. Our other expense for the six-month periods ended June 30, 2025 and 2024 was $6.6 million and $1.7 million, respectively. The increase in other expense for the three and six-month periods ended June 30, 2025 compared to the corresponding periods of 2024 were primarily related to decreased interest income associated with reduced cash and cash equivalent balances, partially offset by a decrease in interest expense as a result of having no outstanding amounts due under the term loan of our Amended Fourth A&R Credit Agreement for the three and six-month periods ended June 30, 2025.

Effective Tax Rate

Our provision for income taxes for the three-month periods ended June 30, 2025 and 2024 was a tax expense of $10.8 million and $10.1 million, respectively, which resulted in an effective tax rate of 24.9% and 22.1%, respectively. Our provision for income taxes for the six-month periods ended June 30, 2025 and 2024 was a tax expense of $18.6 million and $16.2 million, respectively, which resulted in an effective tax rate of 22.9% and 20.2%, respectively. The increase in the effective income tax rate and income tax expense for the three and six-month periods ended June 30, 2025, when compared to the prior-year periods, was primarily due to decreased benefit from discrete items such as share-based compensation and contingent liabilities and increased permanent tax differences in foreign jurisdictions.

Net Income

Our net income for the three-month periods ended June 30, 2025 and 2024 was $32.6 million and $35.7 million, respectively. The decrease in our net income for the three-month period ended June 30, 2025 was the result of several principal factors, including increased SG&A and R&D expenses, other expenses, and income tax expense, partially offset by increased sales and gross margin.

Our net income for the six-month periods ended June 30, 2025 and 2024 was $62.7 million and $64.0 million, respectively. The decrease in our net income for the six-month period ended June 30, 2025 was the result of several principal factors, including increased SG&A and R&D expenses, contingent consideration expense, other expenses, and income tax expense, partially offset by increased sales and gross margin.

LIQUIDITY AND CAPITAL RESOURCES

Capital Commitments, Contractual Obligations and Cash Flows

As of June 30, 2025 and December 31, 2024, our current assets exceeded current liabilities by $697.5 million and $707.4 million, respectively, and we had cash, cash equivalents and restricted cash of $343.9 million and $378.8 million, respectively, of which $69.7 million and $50.6 million, respectively, were held by foreign subsidiaries. We currently believe future repatriation of cash and other property held by our foreign subsidiaries will generally not be subject to U.S. federal income tax. As a result, we are not permanently reinvested with respect to our historic unremitted foreign earnings. In addition, cash held by our subsidiary in China is subject to local laws and regulations that require government approval for the transfer of such funds to entities located outside of China. As of June 30, 2025, and December 31, 2024, we had cash, cash equivalents and restricted cash of $29.2 million and $18.1 million, respectively, within our subsidiary in China.

38

Table of Contents

Cash flows provided by operating activities. We generated cash from operating activities of $123.9 million and $104.7 million during the six-month periods ended June 30, 2025 and 2024, respectively. Significant factors affecting operating cash flows during these periods included:

Net income was $62.7 million and $64.0 million for the six-month periods ended June 30, 2025 and 2024, respectively.
Depreciation and amortization was approximately $60.3 million and $47.7 million for the six-month periods ended June 30, 2025 and 2024, respectively. The increase in depreciation and amortization for the six-month period ended June 30, 2025 was primarily associated with the amortization of developed technology and other intangible assets acquired from EGS, Cook and Biolife.
Cash provided by (used for) inventories was approximately $(11.7) million and $3.1 million for the six-month periods ended June 30, 2025 and 2024, respectively. The increase in inventories during 2025 was principally associated with our strategy to proactively invest in our inventory balances to encourage high customer service levels, as well as to build bridge inventory for production line transfers and increases in safety stock due to vendor supply delays.
Cash (used for) provided by trade payables was $3.7 million and $(7.1) million for the six-month periods ended June 30, 2025 and 2024, respectively, due primarily to the timing of payments.
Stock-based compensation expense was $20.0 million and $12.2 million for the six-month periods ended June 30, 2025 and 2024, respectively. The increase in stock-based compensation expense during 2025 is primarily associated with the increase in the Company’s stock price and grants of restricted stock units.

Cash flows used in investing activities. We used cash in investing activities of $173.0 million and $38.5 million for the six-month periods ended June 30, 2025 and 2024, respectively. We used cash for capital expenditures of property and equipment of $34.8 million and $22.3 million in the six-month periods ended June 30, 2025 and 2024, respectively. Capital expenditures in each period were primarily related to investments in property and equipment to support development and production of our products, and in 2025 includes costs for the construction of a new distribution facility in South Jordan, Utah. Historically, we have incurred significant expenses in connection with facility construction, production automation, product development and the introduction of new products. We anticipate that we will spend approximately $90 to $100 million in 2025 for property and equipment.

Cash outflows for the acquisition of equity investments and issuance of notes receivable were $14.6 million and $9.7 million for the six-month periods ended June 30, 2025 and 2024, respectively. Cash outflows invested in acquisitions were $122.6 million for the six-month period ended June 30, 2025 and were primarily related to the acquisition of Biolife in May 2025. Cash outflows invested in acquisitions were $4.9 million for the six-month period ended June 30, 2024 and were related to the initial payment for the acquisition of assets from SSI and a deferred payment for the acquisition of assets from Restore Endosystems.

Cash flows provided by (used in) financing activities. Cash provided by (used in) financing activities for the six-month periods ended June 30, 2025 and 2024 was $11.3 million and $(14.9) million, respectively. For the six-month period ended June 30, 2024, we had cash used in financing activities primarily attributable to repayment of net borrowings under our Amended Fourth A&R Credit Agreement in an aggregate amount of $24.1 million. We had cash proceeds from the issuance of Common Stock of $20.0 million and $10.9 million for the six-month periods ended June 30, 2025 and 2024, respectively, related to the exercise of non-qualified stock options.

As of June 30, 2025, we had outstanding borrowings of $747.5 million and had issued letter of credit guarantees of $2.9 million, with additional available borrowings of approximately $697 million under the Amended Fourth A&R Credit Agreement, based on the maximum net leverage ratio and the aggregate revolving credit commitment pursuant to the Amended Fourth A&R Credit Agreement. Our interest rate as of June 30, 2025 and December 31, 2024 was a fixed rate of 3.0% on our Convertible Notes.

39

Table of Contents

We currently believe that our existing cash balances, anticipated future cash flows from operations and borrowings under our long-term debt agreements will be adequate to fund our current and currently planned future operations for the next twelve months and the foreseeable future. In the event we pursue and complete significant transactions or acquisitions in the future, additional funds may be required to meet our strategic needs, which may require us to raise additional funds in the debt or equity markets.

CRITICAL ACCOUNTING POLICIES AND ESTIMATES

Our financial results are affected by the selection and application of accounting policies and methods. In the six-month period ended June 30, 2025 there were no changes to the application of critical accounting policies previously disclosed in Part II, Item 7 of our 2024 Annual Report on Form 10-K.

CAUTIONARY NOTICE REGARDING FORWARD-LOOKING STATEMENTS

This report contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). Forward-looking statements include, among others:

statements proceeded or followed by, or that include the words, “may,” “will,” “should,” “expects,” “plans,” “anticipates,” “intends,” “seeks,” “believes,” “estimates,” “projects,” “forecasts,” “potential,” “target,” “continue,” “upcoming,” “optimistic” or other forms of these words or similar words or expressions, or the negative thereof or other comparable terminology;
statements that address our future operating performance or events or developments that we expect or anticipate will occur, including, without limitation, any statements regarding our projected earnings, revenues or other financial measures, our plans and objectives for future operations, our proposed new products or services, the integration, development or commercialization of the business or any assets acquired from other parties, future economic conditions or performance, the implementation of, and results which may be achieved through, Merit’s Continued Growth Initiatives Program or other business optimization initiatives, and any statements of assumptions underlying any of the foregoing; and
statements regarding our past performance, efforts, or results about which inferences or assumptions may be made, including statements proceeded or followed by the words "preliminary," "initial," "potential," "possible," "diligence," "industry-leading," "compliant," "indications," or "early feedback" or other forms of these words or similar words or expressions, or the negative thereof or other comparable terminology.

The forward-looking statements contained in this report are based on our management’s current expectations and assumptions regarding future events or outcomes. If underlying expectations or assumptions prove inaccurate, or risks or uncertainties materialize, actual results will likely differ, and could differ materially, from our expectations reflected in any forward-looking statements. Financial estimates are subject to change and are not intended to be relied upon as predictions of future operating results. Investors are cautioned not to unduly rely on any such forward-looking statements.

The following are some of the important risks and uncertainties that could cause our actual results to differ from our expectations in any forward-looking statements: inherent risks and uncertainties associated with consequences of Merit’s executive succession planning activities and leadership transition; risks and uncertainties regarding trade policies or related actions implemented by the U.S. or other countries, including existing, proposed or prospective tariffs, duties or other measures; inherent risks and uncertainties associated with Merit’s acquisition of Biolife Delaware, L.L.C. (“Biolife”); Merit’s integration of the Biolife business and operations and its ability to achieve revenues and other financial measures consistent with its forecasts projected for the Biolife acquisition; inherent risks and uncertainties associated with Merit’s integration of products acquired from Cook Medical Holdings LLC and Merit’s ability to achieve anticipated financial results, product development and other anticipated benefits of such acquisition; effects of the Convertible Notes on Merit’s net income and earnings per share performance; disruptions in Merit’s supply chain, manufacturing or sterilization processes; U.S. and global political, economic, competitive, reimbursement and regulatory conditions; reduced availability of, and price increases associated with, components and other raw materials; increases in transportation expenses; risks

40

Table of Contents

relating to Merit’s potential inability to successfully manage growth through acquisitions generally, including the inability to effectively integrate acquired operations or products or commercialize technology developed internally or acquired through completed, proposed or future transactions; fluctuations in interest or foreign currency exchange rates and inflation; cybersecurity events; difficulties relating to development, testing and regulatory approval, clearance and maintenance of Merit’s products; the safety, efficacy and patient and physician adoption of Merit’s products; the ability to fully enroll and the outcomes of ongoing and future clinical trials and market studies relating to Merit’s products; modification or limitation of, or policies and procedures associated with, governmental or private insurance reimbursement policies; litigation and other judicial proceedings affecting Merit; consequences associated with a Corporate Integrity Agreement executed between Merit and the U.S. Department of Justice; failure to comply with U.S. and foreign laws and regulations; restrictions on Merit’s liquidity or business operations resulting from its debt agreements; infringement of Merit’s technology or the assertion that Merit’s technology infringes the rights of other parties; product recalls and product liability claims; potential for significant adverse changes in governing regulations; changes in tax laws and regulations in the United States or other jurisdictions or exposure to additional tax liabilities which may adversely affect our effective tax rate; termination of relationships with Merit’s suppliers, or failure of such suppliers to perform; development of new products and technology that could render Merit’s existing or future products obsolete; market acceptance of new products; failure to comply with applicable environmental laws; changes in key personnel; labor shortages and increases in labor costs; price and product competition; extreme weather events; and geopolitical events. For a further discussion of the risks and uncertainties and other factors affecting our business, see Part I, Item 1A. “Risk Factors” in our 2024 Annual Report on Form 10-K filed with the SEC, which we (i) updated in Part II, Item 1A. “Risk Factors” in our Quarterly Report on Form 10-Q for the quarter ended March 31, 2025, (ii) update in Part II, Item 1A. “Risk Factors” in this report, and (iii) may further update in subsequent Quarterly Reports on Form 10-Q that we will file hereafter.

All subsequent forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by these cautionary statements. All forward-looking statements included in this report are made as of the date hereof and are based on information available to us as of such date. We assume no obligation to update any forward-looking statement. If we do update or correct one or more forward-looking statements, investors and others should not conclude that we will make additional updates or corrections.

NOTICE REGARDING TRADEMARKS

This report includes trademarks, tradenames and service marks that are our property or the property of others. Solely for convenience, such trademarks and tradenames sometimes appear without any “™” or “®” symbol. However, failure to include such symbols is not intended to suggest, in any way, that we will not assert our rights or the rights of any applicable licensor, to these trademarks and tradenames.

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

Quantitative and qualitative disclosures about currency exchange rate risk and interest rate risk are included in Part II, Item 7A "Quantitative and Qualitative Disclosures About Market Risk" in the 2024 Annual Report on Form 10-K. In the six-month period ended June 30, 2025, there were no material changes from the information provided therein.

41

Table of Contents

ITEM 4. CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

Our management is responsible for establishing and maintaining adequate disclosure controls and procedures for our company. Consequently, our management, with the participation of our chief executive officer and chief financial officer, evaluated the effectiveness of our disclosure controls and procedures pursuant to Rule 13a-15 under the Exchange Act as of June 30, 2025. In designing and evaluating the disclosure controls and procedures, management recognized that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives. In addition, the design of disclosure controls and procedures must reflect the fact that there are resource constraints, and that management is required to apply its judgment in evaluating the benefits of possible controls and procedures relative to their costs. Based on that evaluation, our chief executive officer and chief financial officer concluded that our disclosure controls and procedures are designed at a reasonable assurance level and are effective to provide reasonable assurance that information we are required to disclose in reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in Securities and Exchange Commission rules and forms, and that such information is accumulated and communicated to our management, including our chief executive officer and chief financial officer, as appropriate, to allow timely decisions regarding required disclosure.

Changes in Internal Control Over Financial Reporting

Except as set forth below, during the quarter ended June 30, 2025, there were no changes in our internal control over financial reporting that materially affected, or were reasonably likely to materially affect, our internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f) under the Securities Exchange Act of 1934).

On May 20, 2025, we completed our acquisition of Biolife, L.L.C. We are currently integrating the policies, processes, employees, technology and operations of Biolife. Management does not currently expect a material change to our internal controls over financial reporting as we fully integrate Biolife. Management will continue to evaluate our internal control over financial reporting as we execute acquisition integration activities.

42

Table of Contents

PART II - OTHER INFORMATION

ITEM 1. LEGAL PROCEEDINGS

See Note 10, Commitments and Contingencies set forth in the notes to our consolidated financial statements included in Part I, Item 1 of this report.

ITEM 1A. RISK FACTORS

In addition to other information set forth in this report, readers should carefully consider the factors discussed in Part I, Item 1A. "Risk Factors" of our 2024 Annual Report on Form 10-K, as updated and supplemented below. Any of the risk factors disclosed in our reports could materially affect our business, financial condition or future results. The risks described here and in our 2024 Annual Report on Form 10-K are not the only risks we face. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may materially and adversely affect our business, financial condition and/or operating results. The discussion of the risk factors below updates the corresponding disclosure under the same heading in the 2024 Annual Report on Form 10-K and may contain material changes to the corresponding risk factor discussion in our 2024 Annual Report on Form 10-K.

Changes in economic and geopolitical conditions, domestic and foreign trade policies, monetary policies and other factors beyond our control may adversely impact our business, operations and financial condition.

Our operations and performance are significantly impacted by global, regional and U.S. economic and geopolitical conditions. The global macroeconomic environment continues to be challenging due to the effects of inflation, instability in global credit markets, uncertainty regarding global central bank monetary policy, instability in the geopolitical environment in many parts of the world, current economic challenges in China, and other factors. Periods of diplomatic or armed conflict, such as the ongoing conflict in Ukraine, tensions in the Middle East and China-Taiwan relations, may result in (i) new and rapidly evolving sanctions and trade restrictions, which may impair trade with sanctioned individuals and countries, and (ii) negative impacts to regional trade ecosystems among our customers, partners, and us. Non-compliance with sanctions, as well as general ecosystem disruptions, could result in reputational harm, operational delays, monetary fines, lost revenues, increased costs, lost export privileges or criminal sanctions.

The U.S. government recently announced changes to its trade policies, including increasing tariffs on imports, in some cases significantly, and potentially negotiating or terminating existing trade agreements. Many of the announced tariffs apply to countries from which we import our raw materials, component parts and finished products, including Mexico, Ireland and China, which could significantly increase our manufacturing costs. The current tariff environment is dynamic and uncertain, as the U.S. government has imposed, modified and paused tariffs multiple times since the beginning of 2025. Changes to tariffs and other trade restrictions can be announced at any time with little or no notice. We cannot predict with certainty the future trade policy of the United States or other countries. We are currently evaluating the potential impact of the imposition of tariffs on our business and financial condition. However, the ultimate impact of any announced or future tariffs will depend on various factors, including (i) whether such tariffs are ultimately implemented, (ii) the timing and duration of implementation and the amount, scope and nature of such tariffs and (iii) potential exclusions from the application of those tariffs.

Additionally, potential tariffs or other U.S. trade policy measures could trigger retaliatory actions by other countries, including by countries that are significant markets for our products, such as China. The escalation of trade tensions could impact Merit in a variety of ways, including (i) increases in manufacturing costs, including with respect to our products manufactured in the U.S., Mexico and Ireland, (ii) disruptions or delays to our global supply chain, (iii) limitations on our ability to sell our products domestically or abroad, and (iv) reductions in sales volumes and gross margins for our products, any of which could negatively affect our business, operations and financial condition.

Furthermore, tariffs or other trade restrictions may lead to continuing uncertainty and volatility in U.S. and global financial and economic conditions and commodity markets, significant inflation, and ultimately reduced demand for our products.   Also, disruptions and volatility in the financial markets may lead to adverse changes in the availability, terms and cost of capital. Such adverse changes could increase our costs of capital and limit our access to external financing sources to fund acquisitions, capital expenditures, or refinancing of debt maturities on similar terms, which could in turn reduce our cash flows and limit our ability to pursue growth opportunities.

43

Table of Contents

The above factors, as well as other economic and geopolitical factors in the U.S. and abroad, could have a material adverse effect on our business, operations and financial condition, including:

changes in economic, monetary and fiscal policies in the U.S. and abroad;
a global or regional economic slowdown in any of our market segments;
public health crises, and government and social responses;
government cost-reduction initiatives, including such initiatives implemented by the Trump administration;
policies in various countries that favor domestic industries or restrict foreign companies;
postponement of spending, in response to tighter credit, financial market volatility and other factors;
rapid escalation of the cost of regulatory compliance and litigation; and
credit risks, longer payment cycles and other challenges in collecting accounts receivable.

If we are unable to effectively execute our leadership succession plans and attract, develop and retain key employees, our business and results of operations could be harmed.

Effective succession planning is critical to our long-term success. Failure to ensure the transfer of knowledge and smooth transitions involving executives and other key employees could hinder our strategic planning and execution. Changes in our management team may be disruptive to our business, and any failure to successfully integrate key new hires or promote employees could adversely affect our operations.

On July 7, 2025, following the conclusion of an extensive search and evaluation process, we announced the appointment of Martha Aronson as Merit’s new President and Chief Executive Officer, effective October 3, 2025. Fred P. Lampropoulos will remain as Chairman of the Board, President and Chief Executive Officer through October 3, 2025, and will continue to serve as Chairman of the Board thereafter. While we seek to manage this leadership transition carefully, changes in leadership are inherently difficult and may negatively impact relationships with key customers, suppliers, investors and employees, cause operational or administrative inefficiencies or disruptions, distract from the achievement of our strategic business objectives, harm our workplace culture, result in loss of institutional knowledge, cause additional volatility in our stock price, or other adverse consequences resulting from the anticipated transition, the occurrence of any of which could have a materially adverse effect on our business.

We do not maintain key man life insurance on Mr. Lampropoulos or Ms. Aronson. The loss of Mr. Lampropoulos, Ms. Aronson, or of certain other key management personnel, could have a materially adverse effect on our business, operations and financial condition.

Our ability to compete effectively depends on our ability to attract, develop and retain executives and key employees. The market for experienced and talented employees, particularly for persons with certain technical competencies, is highly competitive. Inflationary pressures, labor demand and shortages and other macroeconomic factors have increased and could further increase the cost of labor, particularly in Mexico, and could harm our ability to recruit, hire and retain talented employees. Further, if we are unable to maintain (i) competitive and equitable compensation and benefit programs, including incentive programs which reward financial and operational performance, and (ii) an inclusive work culture that aligns our diverse workforce with our mission and values, our ability to recruit, hire, develop, engage, motivate and retain talented and experienced employees could be negatively affected, which could adversely impact our operating results and financial condition.

ITEM 5. OTHER INFORMATION

None of our directors or officers informed us of the adoption or termination of a “Rule 10b5-1 trading arrangement” or “non-Rule 10b5-1 trading arrangement,” as those terms are defined in Item 408 of Regulation S-K, during the three-month period ended June 30, 2025.

44

Table of Contents

ITEM 6. EXHIBITS

Exhibit No.

   

Description

2.1

Agreement and Plan of Merger by and among Merit Medical Systems, Inc., Biolife Transaction Sub, LLC, Biolife, L.L.C., and Shareholder Representative Services LLC, dated as of May 16, 2025.

3.1

Second Amended and Restated Articles of Incorporation.*

3.2

Fourth Amended and Restated Bylaws.*

10.1

Form of Restricted Stock Unit Award Agreement, dated May 15, 2025, by and between Merit Medical Systems, Inc. and each of the following individuals: Lonny J. Carpenter, Stephen C. Evans, David K. Floyd, Thomas J. Gunderson, Laura S. Kaiser, Michael R. McDonnell, F. Ann Millner, Silvia M. Perez and Lynne N. Ward.

19.1

Corporate Policy on Insider Trading (revised May 15, 2025).

31.1

Certification of Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.2

Certification of Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

32.1

Certification of Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

32.2

Certification of Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

101

The following financial information from the quarterly report on Form 10-Q for the quarter ended June 30, 2025, formatted in Inline Extensible Business Reporting Language (iXBRL): (i) Consolidated Balance Sheets, (ii) Consolidated Statements of Income, (iii) Consolidated Statements of Comprehensive Income (iv) Consolidated Statements of Stockholders’ Equity, (v) Consolidated Statements of Cash Flows, and (vi) related Condensed Notes to the Unaudited Consolidated Financial Statements, tagged in detail.

104

 

Cover Page Interactive Data File (the cover page XBRL tags are embedded within the Inline XBRL document).

* These exhibits are incorporated herein by reference.

† Indicates management contract or compensatory plan or arrangement.

45

Table of Contents

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

MERIT MEDICAL SYSTEMS, INC.

Date: July 30, 2025

By:

/s/ FRED P. LAMPROPOULOS

     Fred P. Lampropoulos

     Chief Executive Officer and President

Date: July 30, 2025

By:

/s/ RAUL PARRA

     Raul Parra

     Chief Financial Officer and Treasurer

46


ATTACHMENTS / EXHIBITS

ATTACHMENTS / EXHIBITS

EX-2.1

EX-10.1

EX-19.1

EX-31.1

EX-31.2

EX-32.1

EX-32.2

EX-101.SCH

EX-101.CAL

EX-101.DEF

EX-101.LAB

EX-101.PRE

IDEA: R1.htm

IDEA: R2.htm

IDEA: R3.htm

IDEA: R4.htm

IDEA: R5.htm

IDEA: R6.htm

IDEA: R7.htm

IDEA: R8.htm

IDEA: R9.htm

IDEA: R10.htm

IDEA: R11.htm

IDEA: R12.htm

IDEA: R13.htm

IDEA: R14.htm

IDEA: R15.htm

IDEA: R16.htm

IDEA: R17.htm

IDEA: R18.htm

IDEA: R19.htm

IDEA: R20.htm

IDEA: R21.htm

IDEA: R22.htm

IDEA: R23.htm

IDEA: R24.htm

IDEA: R25.htm

IDEA: R26.htm

IDEA: R27.htm

IDEA: R28.htm

IDEA: R29.htm

IDEA: R30.htm

IDEA: R31.htm

IDEA: R32.htm

IDEA: R33.htm

IDEA: R34.htm

IDEA: R35.htm

IDEA: R36.htm

IDEA: R37.htm

IDEA: R38.htm

IDEA: R39.htm

IDEA: R40.htm

IDEA: R41.htm

IDEA: R42.htm

IDEA: R43.htm

IDEA: R44.htm

IDEA: R45.htm

IDEA: R46.htm

IDEA: R47.htm

IDEA: R48.htm

IDEA: R49.htm

IDEA: R50.htm

IDEA: R51.htm

IDEA: R52.htm

IDEA: R53.htm

IDEA: R54.htm

IDEA: R55.htm

IDEA: R56.htm

IDEA: R57.htm

IDEA: R58.htm

IDEA: R59.htm

IDEA: R60.htm

IDEA: R61.htm

IDEA: R62.htm

IDEA: R63.htm

IDEA: R64.htm

IDEA: R65.htm

IDEA: R66.htm

IDEA: R67.htm

IDEA: R68.htm

IDEA: R69.htm

IDEA: R70.htm

IDEA: R71.htm

IDEA: R72.htm

IDEA: R73.htm

IDEA: FilingSummary.xml

IDEA: MetaLinks.json

IDEA: mmsi-20250630x10q_htm.xml