Home › Device types › NTE
Temporary Carotid Catheter For Embolic Capture
FDA product code NTE · Class 2 · Cardiovascular
72
Registered devices
5,311
Adverse events
30
Recalls
36
510(k) clearances
Devices with this code
ANGIOGUARD — CORDIS CORPORATIONSpiderFX™ — EV3, INCEMBOSHIELD NAV6 — ABBOTT VASCULAR INC.Accunet — ABBOTT VASCULAR INC.EMBOSHIELD NAV6 — ABBOTT VASCULAR INC.Accunet — ABBOTT VASCULAR INC.Wirion Retrieval Catheter — GARDIA MEDICAL LTDANGIOGUARD — CORDIS CORPORATIONSpiderFX™ — EV3, INCVanguard — Contego Medical, Inc.Paladin — Contego Medical, Inc.GORE Embolic Filter — W. L. Gore & Associates, Inc.ENROUTE Transcarotid Neuroprotection System — BOSTON SCIENTIFIC CORPORATIONVanguard — Contego Medical, Inc.GORE Embolic Filter — W. L. Gore & Associates, Inc.ANGIOGUARD — CORDIS CORPORATIONSpiderFX™ — EV3, INCAccunet — ABBOTT VASCULAR INC.ANGIOGUARD — Cordis US Corp.SpiderFX™ — EV3, INCBAREWIRE — ABBOTT VASCULAR INC.Nanoparasol, Peel Away — Microvention, Inc.ANGIOGUARD — CORDIS CORPORATIONENROUTE Transcarotid Neuroprotection System — Silk Road Medical, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-09 | Boston Scientific Corporation | Potential for arterial sheath tip separation or partial tip separation during use. |
| 2026-07-09 | Boston Scientific Corporation | Potential for arterial sheath tip separation or partial tip separation during use. |
| 2023-10-12 | Medtronic Inc | The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and superior sticker, one on each side of the manifold. These stickers label the common |
| 2023-10-12 | Medtronic Inc | The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and superior sticker, one on each side of the manifold. These stickers label the common |
| 2023-10-12 | Medtronic Inc | The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and superior sticker, one on each side of the manifold. These stickers label the common |
| 2023-03-24 | Cordis US Corp | There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pr |
| 2023-03-24 | Cordis US Corp | There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pr |
| 2023-03-24 | Cordis US Corp | There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pr |
| 2023-03-24 | Cordis US Corp | There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pr |
| 2023-03-24 | Cordis US Corp | There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pr |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.