Powerbasetec GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Powerbasetec GmbH - FDA 510(k) Cleared Devices
Recent clearances: ParaMotion
1
Total
1
Cleared
0
Denied
Powerbasetec GmbH has 1 FDA 510(k) cleared medical devices. Based in Bodensee, DE.
Last cleared in 2022. Active since 2022. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Powerbasetec GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qip GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Powerbasetec GmbH
1 devices