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Eyefix, Inc.

Country not established

Devices
1

What Eyefix, Inc. makes

Eyefix, Inc. manufactures ophthalmic examination tools, including the Eye Fixation Speculum, which is designed to hold the eyelids open during eye examinations to improve visibility of the eye’s interior.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Eye Fixation Speculum Ref K964289

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Eyefix, Inc. have in the registry?

The registry currently lists 1 device for Eyefix, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Eyefix, Inc.'s devices?

Among its 1 most recently registered device, Eyefix, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Eyefix, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Eyefix, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Eyefix, Inc. in the registry?

The most recently registered devices listed for Eyefix, Inc. include EYE FIXATION SPECULUM.

Generated automatically from registry data and not verified by a human reviewer.