Medical Device Manufacturer · US , Sunnyvale , CA

Cormatrix Cardiovascular, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2005

Total

Cleared

Denied

Cormatrix Cardiovascular, Inc. has 7 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 7 cleared submissions from 2005 to 2018. Primary specialty: Cardiovascular.

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

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

Cormatrix Cardiovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cormatrix Cardiovascular, Inc.

7 devices

1-7 of 7

Data Source

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

Last updated: Jun 08, 2026