Biotec Italia, Srl - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biotec Italia, Srl has 1 FDA 510(k) cleared medical devices. Based in Dueville (Vi), IT.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biotec Italia, Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Evoskin, LLC as regulatory consultant.
1 devices