Rupiani is one of 289 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Rupiani - FDA 510(k) Cleared Devices
Recent clearances: Weely Manual Wheelchair
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.
510(k) submissions have been managed by Spectre Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Rupiani
1 devices