Intrauma S.P.A is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Intrauma S.P.A - FDA 510(k) Cleared Devices
Recent clearances: WRISTAR MultiAx Distal Radius Kit, KITE Distal Fibula Kit, Elos® Intramedullary Nailing System
3
Total
3
Cleared
0
Denied
Intrauma S.P.A has 3 FDA 510(k) cleared medical devices. Based in Rivoli (To), IT.
Latest FDA clearance: Nov 2025. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Intrauma S.P.A Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and MCRA.
FDA 510(k) Regulatory Record - Intrauma S.P.A
3 devices