Medical Device Manufacturer · US , Claremont , NH

Vertex-Dental B.V. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2010
8
Total
8
Cleared
0
Denied

Vertex-Dental B.V. has 8 FDA 510(k) cleared medical devices. Based in Claremont, US.

Latest FDA clearance: Sep 2024. Active since 2010. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Vertex-Dental B.V. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Vertex-Dental B.V.
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