Medical Device Manufacturer · CH , Epalinges

Distalmotion SA - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 2024

Total

Cleared

Denied

Distalmotion SA has 4 FDA 510(k) cleared medical devices. Based in Epalinges, CH.

Latest FDA clearance: Aug 2026. Active since 2024. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Distalmotion SA is one of 130 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Distalmotion SA

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 05, 2026