Miromatrix Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Miromatrix Medical, Inc. makes
Miromatrix Medical, Inc. manufactures biological meshes and wound matrices, including absorbable and non-absorbable variants for hernia repair and soft tissue reinforcement, as well as dermal substitutes for wound care applications.
These products are classified under FDA Class II and Class III (unclassified) and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Miromatrix Biological Mesh RS Ref K150341
Regimes: 510(k) Registry: 510(k)Miromatrix Biological Mesh TW Ref K162570
Regimes: 510(k) Registry: 510(k)Miromatrix Biological Mesh Ref K134033
Regimes: 510(k) Registry: 510(k)Wound Matrix TF Ref K143426
Regimes: 510(k) Registry: 510(k)Miromatrix Wound Matrix Ref K140510
Regimes: 510(k) Registry: 510(k)Miromatrix Biological Mesh Ref K160400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Miromatrix Medical, Inc. have in the registry?
The registry currently lists 6 devices for Miromatrix Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Miromatrix Medical, Inc.'s devices?
Among its 6 most recently registered devices, Miromatrix Medical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Miromatrix Medical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Miromatrix Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Miromatrix Medical, Inc. in the registry?
The most recently registered devices listed for Miromatrix Medical, Inc. include Miromatrix Biological Mesh RS, Miromatrix Biological Mesh TW, MIROMATRIX BIOLOGICAL MESH and Wound Matrix TF.