Pentaferte S.P.A is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Pentaferte S.P.A - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pentaferte S.P.A has 2 FDA 510(k) cleared medical devices. Based in Campli (Teramo), IT.
Historical record: 2 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pentaferte S.P.A Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pentaferte S.P.A
2 devices