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Mossimo, Inc.

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Devices
1

What Mossimo, Inc. makes

Mossimo, Inc. manufactures the Mossimo Optic Eyeware, a Class I medical device designed for optical correction and vision enhancement.

The Mossimo Optic Eyeware is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in 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

  • Mossimo Optic Eyewear Ref K912509

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

Frequently asked questions

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

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

Which registries list Mossimo, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Mossimo, Inc. include MOSSIMO OPTIC EYEWEAR.

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