Biedermann Motech GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Biedermann Motech GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: MOSS VRS Spinal System, MOSS VRS Spinal System
4
Total
4
Cleared
0
Denied
Biedermann Motech GmbH & Co. KG has 4 FDA 510(k) cleared medical devices. Based in Villingen-Schwenningen, DE.
Last cleared in 2021. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biedermann Motech GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biedermann Motech GmbH & Co. KG
4 devices