Medical Device Manufacturer · FR , Antony

Moria SA

5 submissions · 5 cleared · Since 2002
5
Total
5
Cleared
0
Denied

Moria SA — FDA 510(k) Submissions

Moria SA has submitted 5 FDA 510(k) premarket notifications since 2002, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Keratome, Ac-powered, Keratome, Battery-powered . Use the specialty filter in the sidebar to narrow results.

5 devices
1–5 of 5
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All5 Ophthalmic 5