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Altair Eyewear

Country not established

Devices
1

What Altair Eyewear makes

Altair Eyewear manufactures eyewear frames, including designs intended for prescription and non-prescription use. These products are primarily structured for optical and non-optical applications, such as corrective lenses and fashion eyewear.

The company’s eyewear frames are classified as Class I medical devices under FDA regulations, with some models subject to 510(k) clearance for specific indications. The products are listed in the FDA’s regulatory database, and the manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Altair Eyewear Frames Ref K931135

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Altair Eyewear have in the registry?

The registry currently lists 1 device for Altair Eyewear. Devices recorded under merged duplicate company entries are counted once.

Which registries list Altair Eyewear's devices?

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

What risk classes do Altair Eyewear's devices fall under?

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

What are the newest devices from Altair Eyewear in the registry?

The most recently registered devices listed for Altair Eyewear include ALTAIR EYEWEAR FRAMES.

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