Medical Device Manufacturer · DE , Vs-Schwenningen

Biedermann Motech GmbH - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1990
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.

FDA 510(k) Regulatory Record - Biedermann Motech GmbH
2 devices
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