Home › Device types › OGI
Nasal Endotracheal Tube Holder Kit
FDA product code OGI · Class 1 · Anesthesiology
13
Registered devices
1
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
RingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCCuraplex — BOUND TREE MEDICAL, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLCRingLoc Hip System — Biomet Orthopedics, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-27 | Medline Industries, LP | Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for applicat |
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.
