Hans Hermann GmbH is one of 516 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: HANS HERMANN LAPAROSCOPES AND ACCESSORIES, 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: Dental.
Browse the FDA 510(k) cleared devices submitted by Hans Hermann GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hans Hermann GmbH
2 devices