Biedermann Motech GmbH - FDA 510(k) Cleared Devices
2
Total
1
Cleared
0
Denied
Biedermann Motech GmbH has 1 FDA 510(k) cleared medical devices. Based in Vs-Schwenningen, DE.
Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biedermann Motech GmbH Filter by specialty or product code using the sidebar.
2 devices