Home › Device types › FGS
Carrier, Sponge, Endoscopic
FDA product code FGS · Class 2 · Gastroenterology, Urology
1
Registered devices
2
Adverse events
1
Recalls
4
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-09-29 | Stryker Endoscopy | Product may not adequately visualize IR light emitted from U- and E- kits due to a manufacturing error. |
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.