Medical Device Manufacturer · IT , Due Carrare Padova

Artiglass Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Artiglass Srl has 2 FDA 510(k) cleared medical devices. Based in Due Carrare Padova, IT.

Last cleared in 2022. Active since 2013. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Artiglass Srl Filter by specialty or product code using the sidebar.

Artiglass Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Artiglass Srl

2 devices

1-2 of 2