Utensili Super Abrasivi is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Utensili Super Abrasivi - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Utensili Super Abrasivi has 1 FDA 510(k) cleared medical devices. Based in (Milan), Italy, IT.
Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Utensili Super Abrasivi Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Utensili Super Abrasivi
1 devices