Resitu Medical AB - FDA 510(k) Cleared Devices

Resitu Medical AB has 1 FDA 510(k) cleared medical devices. Based in Uppsala, SE.

Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Resitu Medical AB Filter by specialty or product code using the sidebar.

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