Resitu Medical AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Resitu Medical AB - FDA 510(k) Cleared Devices
Recent clearances: Resitu Slider 09 (RESL09)
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Resitu Medical AB
1 devices