Dentalpoint AG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Dentalpoint AG has 4 FDA 510(k) cleared medical devices. Based in Dundas, CA.
Historical record: 4 cleared submissions from 2014 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentalpoint AG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dentalpoint AG
4 devices
Cleared
Nov 16, 2018
Zeramex(R) XT Dental Implant System, NobelPearl Dental Implant System
Dental
297d
Cleared
Nov 30, 2016
Zeramex P6 Dental Implant System
Dental
30d
Cleared
Jul 27, 2016
Zeramex P6 Dental Implant System
Dental
338d
Cleared
Aug 12, 2014
ZERAMEX T AND ZERAMEX PLUS DENTAL IMPLANT SYSTEMS
Dental
293d