FDA Device Intelligence
HomeDevice types › FEB

Accessories, Cleaning, For Endoscope

FDA product code FEB · Class 2 · Gastroenterology, Urology

669
Registered devices
5,046
Adverse events
40
Recalls
57
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasXXX
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

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