Adler Ortho S.P.A is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Adler Ortho S.P.A - FDA 510(k) Cleared Devices
Recent clearances: Pantheon Proximal Femur Reconstruction (PFR) System
1
Total
1
Cleared
0
Denied
Adler Ortho S.P.A has 1 FDA 510(k) cleared medical devices. Based in Cormano (Mi), IT.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Adler Ortho S.P.A Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Adler Ortho S.P.A
1 devices