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Stent, Renal
FDA product code NIN · Class 3 · Unknown
104
Registered devices
874
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Herculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Formula 418 — COOK INCORPORATEDHerculink Elite — ABBOTT VASCULAR INC.Formula 418 — COOK INCORPORATEDHerculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Express® SD Renal/Biliary — BOSTON SCIENTIFIC CORPORATIONHerculink Elite — ABBOTT VASCULAR INC.Formula — William Cook Europe ApSHerculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.Formula — William Cook Europe ApSFormula 418 — COOK INCORPORATEDFormula — William Cook Europe ApSExpress® SD Renal/Biliary — BOSTON SCIENTIFIC CORPORATIONFormula — William Cook Europe ApSHerculink Elite — ABBOTT VASCULAR INC.Formula 418 — COOK INCORPORATEDHerculink Elite — ABBOTT VASCULAR INC.Herculink Elite — ABBOTT VASCULAR INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-04-15 | Cook Inc. | The firm received complaints on five devices from one specific lot where the stent dislodged from the balloon delivery system prior to deployment. Use of affect |
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