Msi France is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Msi France - FDA 510(k) Cleared Devices
Recent clearances: SPI Dental Implant System
1
Total
1
Cleared
0
Denied
Msi France has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Msi France Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Msi France
1 devices