Blueshine Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Blueshine Srl - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Blueshine Srl has 3 FDA 510(k) cleared medical devices. Based in Mestre, Venice, IT.
Historical record: 3 cleared submissions from 2006 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Blueshine Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Blueshine Srl
3 devices