Medical Device Manufacturer · US , San Leandro , CA

Mercator Medsystems, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Mercator Medsystems, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Leandro, US.

Last cleared in 2021. Active since 2006. Primary specialty: Cardiovascular.

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

Regulatory submissions have been managed by Target Health, Inc. and Regulatory Technology Services, LLC.

Mercator Medsystems, Inc. is one of 16294 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mercator Medsystems, Inc.

5 devices

1-5 of 5

Data Source

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

Last updated: May 23, 2026