Ceraroot SL is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Ceraroot SL - FDA 510(k) Cleared Devices
Recent clearances: CeraRoot TL Implant System (TL)
1
Total
1
Cleared
0
Denied
Ceraroot SL has 1 FDA 510(k) cleared medical devices. Based in Les Franqueses Del Valles, ES.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ceraroot SL Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ceraroot SL
1 devices