Medical Device Manufacturer · US , Denver , CO

Voco GmbH - FDA 510(k) Cleared Devices

119 submissions · 119 cleared · Since 1991

Recent clearances: VOCO Profluorid Varnish + BioMin, Grandio disc multicolor, Bifix Veneer LC, Bifix Veneer Try-In

119
Total
119
Cleared
0
Denied

Voco GmbH has 119 FDA 510(k) cleared dental devices. Based in Denver, US.

Latest FDA clearance: May 2026. Active since 1991.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Voco GmbH

119 devices
1-12 of 119

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