Intrauma S.P.A - FDA 510(k) Cleared Devices
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.
3 devices