Medical Device Manufacturer · US , Los Angeles , CA

Dentca, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2015

Total

Cleared

Denied

Dentca, Inc. has 6 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Jul 2026. Active since 2015. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dentca, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Denterprise International, Inc. and The 510k Consulting, LLC.

Dentca, Inc. is one of 16079 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dentca, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Aug 06, 2026