Medical Device Manufacturer · ES , Madrid

Xplora 3D Europe S.L - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
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
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