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Cordis US Corporation

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories5
Latest FDA decision2026-06-23
TypeNumberDevice NameCodeDateActions
PMA P100013 Device, hemostasis, vascularMGB2026-06-23 View
PMA P030047 Stent, carotidNIM2026-06-05 View
PMA P040044 Device, hemostasis, vascularMGB2026-05-14 View
PMA P020036 STENT, ILIACNIO2026-01-08 View
PMA P120002 STENT, SUPERFICIAL FEMORAL ARTERYNIP2026-01-08 View
PMA P150002 SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENTMIH2025-05-15 View
PMA P890017 STENT, ILIACNIO2022-12-20 View

Related Clinical Trials

NCT03923387Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure DeviceCOMPLETEDNCT07246902Mobilization and Outcomes After Venous ClosureACTIVE_NOT_RECRUITING
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