Hans Hermann GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Hans Hermann GmbH - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Hans Hermann GmbH
2 devices