FDA Device Intelligence
HomeDevice types › KNF

Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

FDA product code KNF · Class 2 · Obstetrics/Gynecology

304
Registered devices
404
Adverse events
5
Recalls
44
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-02-12Integra LifeSciences Corp.Addendum to the Instructions for Use. The addendum emphasizes the warnings and precautions already contained in the device's IFU and also provides additional wa
2012-05-23Integra LimitedThe Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were released with internal component out of specification.
2009-12-01LINA Medical ApSPotential for the LiNA Loop to break during operating procedure.
2009-12-01LINA Medical ApSPotential for the LiNA Loop to break during operating procedure.
2009-12-01LINA Medical ApSPotential for the LiNA Loop to break during operating procedure.

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.