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Cordis US Corp

21 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO recall (Z-1510-2025)Cordis US Corp2025-04-03
Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO recall (Z-1511-2025)Cordis US Corp2025-04-03
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding cathete recall (Z-1330-2025)Cordis US Corp2025-03-13
MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and recall (Z-0674-2024)Cordis US Corp2024-01-05
MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial a recall (Z-0675-2024)Cordis US Corp2024-01-05
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac cath recall (Z-0286-2024)Cordis US Corp2023-11-09
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC recall (Z-1483-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC recall (Z-1484-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC recall (Z-1485-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC recall (Z-1486-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC recall (Z-1487-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC recall (Z-1488-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC recall (Z-1489-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM recall (Z-1490-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE recall (Z-1491-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE recall (Z-1492-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE recall (Z-1493-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM recall (Z-1494-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM recall (Z-1495-2023)Cordis US Corp2023-05-11
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE recall (Z-1496-2023)Cordis US Corp2023-05-11
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector t recall (Z-0720-2023)Cordis US Corp2022-12-16

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Every clearance here is in the API, with alerts when new ones post.