Medical Device Manufacturer · US , Monson , MA

Numedis, Inc.

1 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

Numedis, Inc. — FDA 510(k) Submissions

Numedis, Inc. has submitted 1 FDA 510(k) premarket notifications since 2007, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Corneal Storage . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

LIFE4C

K063304 · LYX Media, Corneal Storage · Ophthalmic

Dec 2007 415d

Numedis, Inc.

Numedis, Inc. — FDA 510(k) Submissions

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