Leaseir Technologies, Slu is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Leaseir Technologies, Slu - FDA 510(k) Cleared Devices
Recent clearances: Leaseir MHR Xcell (console) (MHR-100b), Leaseir MHR Xcell
2
Total
2
Cleared
0
Denied
Leaseir Technologies, Slu has 2 FDA 510(k) cleared medical devices. Based in Gij?n, ES.
Latest FDA clearance: May 2026. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Leaseir Technologies, Slu Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Freyr Global Regulatory Solutions and Services and Paladin Medical, Inc..
FDA 510(k) Regulatory Record - Leaseir Technologies, Slu
2 devices