FDA Device Intelligence
HomeDevice types › LNZ

Changer, Tube, Endotracheal

FDA product code LNZ · Class 2 · Anesthesiology

31
Registered devices
39
Adverse events
3
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-02-12Sarnova HC, LlcEndotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secu
2024-02-12Sarnova HC, LlcEndotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secu
2006-09-27Teleflex MedicalBiological indicator failed. Investigation eliminated all equipment and product related factors.

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.