Biegler GmbH is one of 22419 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biegler GmbH - FDA 510(k) Cleared Devices
Recent clearances: Stivax, P-STIM, BW685, BW685S
3
Total
3
Cleared
0
Denied
Biegler GmbH has 3 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Biegler GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Promedic, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biegler GmbH
3 devices