Xplora 3D Europe S.L is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Xplora 3D Europe S.L - FDA 510(k) Cleared Devices
Recent clearances: Fas Aligner System
1
Total
1
Cleared
0
Denied
Xplora 3D Europe S.L has 1 FDA 510(k) cleared medical devices. Based in Madrid, ES.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Xplora 3D Europe S.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance4Devices as regulatory consultant.
FDA 510(k) Regulatory Record - Xplora 3D Europe S.L
1 devices