Hans Hermann GmbH

Hans Hermann GmbH holds 2 FDA 510(k) medical device clearances, first cleared 1998, most recent 2005.

Top product codes for Hans Hermann GmbH

GCJ — Gastroenterology, Urology1 device
JEY — Dental1 device

Recent clearances by Hans Hermann GmbH

K051610 — HANS HERMANN LAPAROSCOPES AND ACCESSORIESCode GCJ·2005-07-29
K983535 — THE TITANIUM MINIPLATING SYSTEM, THE TITANIUM MICROPLATING SYSTEM, THE TITANIUM MEDIUMPLATING SYSTEM, MODEL #'S H12-1010Code JEY·1998-12-29

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