Medical Device Manufacturer · DE , Barbing

Aktormed GmbH - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

Aktormed GmbH has 4 FDA 510(k) cleared medical devices. Based in Barbing, DE.

Latest FDA clearance: Aug 2024. Active since 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Aktormed GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Micro-Epsilon America as regulatory consultant.

Aktormed GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Aktormed GmbH

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 10, 2026