Medical Device Manufacturer · NL , Vierpolders

Vitreq BV

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

Vitreq BV — FDA 510(k) Submissions

Vitreq BV has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Photocoagulator And Accessories, Unit, Cryophthalmic . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ophthalmic 2