Ergoline GmbH is one of 470 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, ERGOSELECT/GE, ERGOSELECT 100 K/P, ERGOSELECT 200 K/P
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.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ergoline GmbH
3 devices