Pierenkemper GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Pierenkemper GmbH - FDA 510(k) Cleared Devices
Recent clearances: StimaWELL 120MTRS
1
Total
1
Cleared
0
Denied
Pierenkemper GmbH has 1 FDA 510(k) cleared medical devices. Based in Ehringshausen, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Pierenkemper GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Pierenkemper GmbH
1 devices