Dimar S.P.A. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Dimar S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: Family of DIMAR DMAX NIV masks
1
Total
1
Cleared
0
Denied
Dimar S.P.A. has 1 FDA 510(k) cleared medical devices. Based in Medolla, IT.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dimar S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dimar S.P.A.
1 devices