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Stent, Iliac Vein

FDA product code QAN · Class 3 · Unknown

200
Registered devices
1,289
Adverse events
9
Recalls
0
510(k) clearances

Devices with this code

Zilver Vena — COOK IRELAND LTDVenovo® — Angiomed GmbH & Co. Medizintechnik KGVenovo® — Angiomed GmbH & Co. Medizintechnik KGVICI RDS™ Venous Stent System — Veniti IncVICI RDS™ Venous Stent System — Veniti IncVenovo® — Angiomed GmbH & Co. Medizintechnik KGVenovo® — Angiomed GmbH & Co. Medizintechnik KGAbre™ — MEDTRONIC, INC.Venovo® — Angiomed GmbH & Co. Medizintechnik KGAbre™ — MEDTRONIC, INC.Abre™ — MEDTRONIC, INC.Venovo® — Angiomed GmbH & Co. Medizintechnik KGVENOUS WALLSTENT™ — BOSTON SCIENTIFIC CORPORATIONZilver Vena — COOK IRELAND LTDVenovo® — Angiomed GmbH & Co. Medizintechnik KGZilver Vena — COOK IRELAND LTDVenovo® — Angiomed GmbH & Co. Medizintechnik KGVenovo® — Angiomed GmbH & Co. Medizintechnik KGVICI RDS™ Venous Stent System — Veniti IncVenovo® — Angiomed GmbH & Co. Medizintechnik KGVenovo® — Angiomed GmbH & Co. Medizintechnik KGVenovo® — Angiomed GmbH & Co. Medizintechnik KGAbre™ — MEDTRONIC, INC.Venovo® — Angiomed GmbH & Co. Medizintechnik KG

Recent recalls

DateFirmReason
2025-12-04Medtronic IncStents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in sten
2024-02-16Medtronic Inc.There is a potential for sterile package breach.
2021-11-19Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)There have been reports of stent migration.
2021-04-12Boston Scientific CorporationThe firm has received reports of stent migration after implantation
2021-04-12Boston Scientific CorporationThe firm has received reports of stent migration after implantation
2021-03-16Medtronic Inc.Incorrect size printed on the device; packaging is labeled correctly.
2020-12-14Bard Peripheral Vascular IncReports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
2020-12-14Bard Peripheral Vascular IncReports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
2020-12-14Bard Peripheral Vascular IncReports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.