Ergoline GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ergoline GmbH - FDA 510(k) Cleared Devices
Recent clearances: ers2 - ergoline Rehabilitation System
3
Total
3
Cleared
0
Denied
Ergoline GmbH has 3 FDA 510(k) cleared medical devices. Based in Bitz, B-W, DE.
Last cleared in 2022. Active since 2006. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Ergoline GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ergoline GmbH
3 devices