Medical Device Manufacturer · US , Irvine , CA

Crossbay Medical, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

Crossbay Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 3 cleared submissions from 2014 to 2017. Primary specialty: Obstetrics & Gynecology.

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

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

Crossbay Medical, Inc. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Crossbay Medical, Inc.

3 devices

1-3 of 3

Data Source

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

Last updated: Sep 19, 2026