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Uvbiotek, LLC

United StatesFDA applicant, unverified

Devices
2

What Uvbiotek, LLC makes

Uvbiotek, LLC makes LED light therapy devices and photodynamic therapy devices.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • LED Light Therapy Device Ref K180900

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Photodynamic Therapy Device Ref K170187

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

Frequently asked questions

How many devices does Uvbiotek, LLC have in the registry?

The registry currently lists 2 devices for Uvbiotek, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Uvbiotek, LLC's devices?

Among its 2 most recently registered devices, Uvbiotek, LLC has devices listed in FDA 510(k) (2 devices).

What risk classes do Uvbiotek, LLC's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Uvbiotek, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Uvbiotek, LLC in the registry?

The most recently registered devices listed for Uvbiotek, LLC include LED Light Therapy Device and Photodynamic Therapy Device.

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