Biegler GmbH is one of 4788 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biegler GmbH - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Biegler GmbH
3 devices