T.F.I. System S.R.L is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
T.F.I. System S.R.L - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
T.F.I. System S.R.L has 1 FDA 510(k) cleared medical devices. Based in Roma (Rm), IT.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by T.F.I. System S.R.L Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - T.F.I. System S.R.L
1 devices