Distalmotion SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Distalmotion SA - FDA 510(k) Cleared Devices
Recent clearances: Dexter L6 System, Dexter L6 System
4
Total
3
Cleared
1
Denied
Distalmotion SA has 3 FDA 510(k) cleared medical devices. Based in Epalinges, CH.
Latest FDA clearance: Jun 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.
FDA 510(k) Regulatory Record - Distalmotion SA
4 devices