Sportarredo Group S.C. is one of 223 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Sportarredo Group S.C. - FDA 510(k) Cleared Devices
Recent clearances: HPO Exotic, LP1, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega Lux, BPhase, HPO Exotic, LPI, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega Lux
2
Total
2
Cleared
0
Denied
Sportarredo Group S.C. has 2 FDA 510(k) cleared medical devices. Based in Gruaro, IT.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sportarredo Group S.C. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Registrar Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Sportarredo Group S.C.
2 devices