Pentaferte Italia S.R.L. is one of 212 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Pentaferte Italia S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Pentaflush, ENFit enteral syringes (NUTRIFIT), ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT
3
Total
3
Cleared
0
Denied
Pentaferte Italia S.R.L. has 3 FDA 510(k) cleared medical devices. Based in Campli, IT.
Last cleared in 2022. Active since 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pentaferte Italia S.R.L. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Pentaferte, S.R.L., Vygon USA and Pqe US.
FDA 510(k) Regulatory Record - Pentaferte Italia S.R.L.
3 devices