Rupiani is one of 153 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Rupiani - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rupiani has 1 FDA 510(k) cleared medical devices. Based in Vaudex En Velin, FR.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rupiani Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rupiani
1 devices