Triworks Group Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Triworks Group Srl - FDA 510(k) Cleared Devices
Recent clearances: AgeJet, Medical RF
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.
Regulatory submissions have been managed by Elexes and Neoconcepts, LLC.
FDA 510(k) Regulatory Record - Triworks Group Srl
2 devices