Medical Device Manufacturer · US , Alexandria , VA

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

6 submissions · 6 cleared · Since 2014

Total

Cleared

Denied

Miromatrix Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Alexandria, US.

Historical record: 6 cleared submissions from 2014 to 2017. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Biologics Consulting Group, Inc. as regulatory consultant.

Miromatrix Medical, Inc. is one of 18354 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Data Source

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

Last updated: Sep 20, 2026