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Applied Optic Kinetics, Ltd.

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Devices
1

What Applied Optic Kinetics, Ltd. makes

Applied Optic Kinetics, Ltd. manufactures the NUTRA-TONE 500, a device designed for optical or kinetic therapy applications, likely targeting vision correction or eye alignment support.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The NUTRA-TONE 500 is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Nutra-Tone 500 Ref K833808

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

Frequently asked questions

How many devices does Applied Optic Kinetics, Ltd. have in the registry?

The registry currently lists 1 device for Applied Optic Kinetics, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Applied Optic Kinetics, Ltd.'s devices?

Among its 1 most recently registered device, Applied Optic Kinetics, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Applied Optic Kinetics, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Applied Optic Kinetics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Applied Optic Kinetics, Ltd. in the registry?

The most recently registered devices listed for Applied Optic Kinetics, Ltd. include NUTRA-TONE 500.

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