Kls Martin GmbH + Co. KG

Kls Martin GmbH + Co. KG holds 2 FDA 510(k) medical device clearances, first cleared 2008, most recent 2019.

Top product codes for Kls Martin GmbH + Co. KG

GEI — General, Plastic Surgery2 devices

Recent clearances by Kls Martin GmbH + Co. KG

K183526 — Codman Electrosurgical Generator, Foot PedalCode GEI·2019-04-11
K081678 — CONMED BEAMER SYSTEM C600Code GEI·2008-07-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.