Zeppelin GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Zeppelin GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Zeppelin GmbH has 2 FDA 510(k) cleared medical devices. Based in West Germany, DE.
Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Zeppelin GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zeppelin GmbH
2 devices