Blueshine Srl is one of 223 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Blueshine Srl - FDA 510(k) Cleared Devices
Recent clearances: BLUESHINE'S GOLD SERIES, BLUESHINE GOLD SERIES, BLUESHINE LIGHT SHINE SYSTEMS, SP, TWIN AND COMPACT SP
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Blueshine Srl
3 devices