Distalmotion SA - FDA 510(k) Cleared Devices
3
Total
2
Cleared
1
Denied
Distalmotion SA has 2 FDA 510(k) cleared medical devices. Based in Epalinges, CH.
Latest FDA clearance: Sep 2025. 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.
3 devices