Hans Hermann GmbH is one of 309 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Hans Hermann GmbH - FDA 510(k) Cleared Devices
Recent clearances: THE TITANIUM MINIPLATING SYSTEM, THE TITANIUM MICROPLATING SYSTEM, THE TITANIUM MEDIUMPLATING SYSTEM, MODEL #'S H12-1010
2
Total
2
Cleared
0
Denied
Hans Hermann GmbH has 2 FDA 510(k) cleared medical devices. Based in Wurmlingen, DE.
Historical record: 2 cleared submissions from 1998 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hans Hermann GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hans Hermann GmbH
2 devices