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Nu Photonics, Inc.

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Devices
1

What Nu Photonics, Inc. makes

Nu Photonics, Inc. manufactures the MU Photonics Pain Therapist, a device designed for non-invasive pain management using photonics technology.

The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. 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

  • Mu Photonics Pain Therapist Ref K012508

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

Frequently asked questions

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

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

Which registries list Nu Photonics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Nu Photonics, Inc. include MU PHOTONICS PAIN THERAPIST.

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