Voco GmbH - FDA 510(k) Cleared Devices
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.
119 devices
Cleared
May 01, 2026
VOCO Profluorid Varnish + BioMin
Dental
303d
Cleared
Apr 27, 2026
Grandio disc multicolor
Dental
3d
Cleared
Mar 20, 2026
Bifix Veneer LC, Bifix Veneer Try-In
Dental
214d
Cleared
Jul 03, 2025
MTA vpt
Dental
59d
Cleared
May 21, 2025
GrandioSO Unlimited
Dental
29d
Cleared
Dec 01, 2023
AlignerFlow LC
Dental
163d
Cleared
Jul 31, 2023
V-Print c&b temp
Dental
60d
Cleared
Jul 13, 2023
Admira Fusion 5
Dental
105d
Cleared
Sep 21, 2022
V-Print dentbase
Dental
237d
Cleared
Aug 23, 2022
Bifix Hybrid Abutment Cement
Dental
172d
Cleared
Jul 05, 2022
CediTEC
Dental
113d
Cleared
Dec 09, 2021
VOCO Retraction Paste
Dental
73d
Looking for a specific device from Voco GmbH? Search by device name or K-number.
Search all Voco GmbH devices