Medical Device Manufacturer · FR , Antony

Moria, Inc.

4 submissions · 4 cleared · Since 1998
4
Total
4
Cleared
0
Denied

Moria, Inc. — FDA 510(k) Submissions

Moria, Inc. has submitted 4 FDA 510(k) premarket notifications since 1998, of which 4 received clearance as substantially equivalent to a predicate device.

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

4 devices
1–4 of 4
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All4 Ophthalmic 4