Miromatrix Medical, Inc. is one of 4732 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Miromatrix Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
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.
FDA 510(k) Regulatory Record - Miromatrix Medical, Inc.
6 devices
Cleared
Feb 16, 2017
Miromatrix Biological Mesh TW
General & Plastic Surgery
154d
Cleared
Jun 08, 2016
Miromatrix Biological Mesh
General & Plastic Surgery
117d
Cleared
May 12, 2015
Miromatrix Biological Mesh RS
General & Plastic Surgery
90d
Cleared
Jan 27, 2015
Wound Matrix TF
General & Plastic Surgery
57d
Cleared
Jun 19, 2014
MIROMATRIX WOUND MATRIX
General & Plastic Surgery
111d
Cleared
Mar 31, 2014
MIROMATRIX BIOLOGICAL MESH
General & Plastic Surgery
90d