Triworks Group Srl - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Triworks Group Srl has 2 FDA 510(k) cleared medical devices. Based in Campobasso, IT.
Last cleared in 2022. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Triworks Group Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Neoconcepts, LLC as regulatory consultant.
2 devices