FDA Device Intelligence
HomeDevice types › KAL

Retractor, Ent

FDA product code KAL · Class 1 · Ear, Nose, Throat

1,279
Registered devices
15
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-05-25TELEFLEX LLCThere are incomplete pre-cleaning instructions within the Instructions for Use (IFU).

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.