Medical Device Manufacturer · US , Escondido , CA

Datrix - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Datrix has 5 FDA 510(k) cleared medical devices. Based in Escondido, US.

Historical record: 5 cleared submissions from 1992 to 2005. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Datrix is one of 24105 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Datrix

5 devices

1-5 of 5

Data Source

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

Last updated: Sep 09, 2026