Msi is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Msi - FDA 510(k) Cleared Devices
Recent clearances: DURAMESH Mesh Suture
1
Total
1
Cleared
0
Denied
Msi has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Msi Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Msi
1 devices