Medical Device Manufacturer · US , Farmingdale , NY

Maxi-Aids, Inc.

2 submissions · 2 cleared · Since 1996
2
Total
2
Cleared
0
Denied

Maxi-Aids, Inc. — FDA 510(k) Submissions

Maxi-Aids, Inc. has submitted 2 FDA 510(k) premarket notifications since 1996, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hearing Aid, Group And Auditory Trainer, System, Measurement, Blood-pressure, Non-invasive . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ear, Nose, Throat 1 Cardiovascular 1