Cordis US Corp
Cordis US Corp holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2024, with 22 FDA device recalls on record.
Top product codes for Cordis US Corp
FDA recalls by Cordis US Corp
10 most recent of 22- Z-1510-2025 — Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
- Z-1511-2025 — Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only
- Z-1330-2025 — Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
- Z-0675-2024 — MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites
- Z-0674-2024 — MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.
- Z-0286-2024 — Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
- Z-1487-2023 — ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
- Z-1484-2023 — ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
- Z-1492-2023 — ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
- Z-1493-2023 — ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Cordis US Corp
Data sourced from openFDA. This site is unofficial and independent of the FDA.