Home › Device types › FEI
Instrument, Special Lens, For Endoscope
FDA product code FEI · Class 1 · Gastroenterology, Urology
30
Registered devices
19
Adverse events
2
Recalls
2
510(k) clearances
Devices with this code
NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.Autoclavable HD-Zoom Coupler — W.O.M. World of Medicine GmbHNA — Smith & Nephew, Inc.gastroduodenal FTRD prOVE Cap — Ovesco Endoscopy AGNA — Smith & Nephew, Inc.Arthrex® — ARTHREX, INC.N/A — Smith & Nephew, Inc.N/A — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.Zoom coupler Arthrex 14-29mm C-Mount — W.O.M. World of Medicine GmbHNA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.FTRD prOVE Cap — Ovesco Endoscopy AGNA — Smith & Nephew, Inc.N/A — Smith & Nephew, Inc.INTELIJET — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-10-04 | Medtronic | Product sterility is compromised due to breach of the sterile barrier |
| 2016-10-04 | Medtronic | Product sterility is compromised due to breach of the sterile barrier |
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.