Medical Device Manufacturer · IT , Campli

Pentaferte Italia S.R.L. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

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.

3 devices

1–3 of 3

Data Source

FDA 510(k) public files . 174,402 total devices indexed.