Vitreq BV is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Vitreq BV - FDA 510(k) Cleared Devices
Recent clearances: CryoTreQ, Vitreq disposable laser probes, light fibers and Chandelier
2
Total
2
Cleared
0
Denied
Vitreq BV has 2 FDA 510(k) cleared medical devices. Based in Vierpolders, NL.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vitreq BV Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Beaver-Visitec International, Inc. and Dynamic Strategies, Inc..
FDA 510(k) Regulatory Record - Vitreq BV
2 devices