FDA Device Intelligence
HomeDevice types › OHO

First Aid Kit Without Drug

FDA product code OHO · Class 1 · General, Plastic Surgery

2,310
Registered devices
5
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-07-07INTEGRATED MEDCRAFT LLCDevices could potentially contain an occluded or partially occluded Guedel Airway tip.

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.