Molecular Matrix, Inc. is one of 20069 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Molecular Matrix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Osteo-P Bone Graft Substitute
1
Total
1
Cleared
0
Denied
Molecular Matrix, Inc. has 1 FDA 510(k) cleared medical devices. Based in West Sacramento, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Molecular Matrix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Molecular Matrix, Inc.
1 devices