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Rainbow Optics, Inc.

United StatesFDA applicant, unverified

Devices
2

What Rainbow Optics, Inc. makes

Rainbow Optics, Inc. manufactures spectacle frames and sunglasses designed for optical and protective eyewear applications.

These products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Frames, Spectacle Ref K932813

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Sunglasses Ref K934277

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

Frequently asked questions

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

The registry currently lists 2 devices for Rainbow Optics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rainbow Optics, Inc.'s devices?

Among its 2 most recently registered devices, Rainbow Optics, Inc. has devices listed in FDA 510(k) (2 devices).

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

Among its 2 most recently registered devices, the classes recorded for Rainbow Optics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Rainbow Optics, Inc. include FRAMES, SPECTACLE and SUNGLASSES.

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