Medical Device Manufacturer · CA , Dundas

Dentalpoint AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

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.

510(k) submissions have been managed by Mapi USA, Inc. as regulatory consultant.

Dentalpoint AG is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dentalpoint AG

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Jun 08, 2026