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Genesis Health Light Corporation

CanadaFDA applicant, unverified

Devices
1

What Genesis Health Light Corporation makes

Genesis Health Light Corporation manufactures the CS1000, a light therapy device designed for medical applications requiring controlled phototherapy.

The CS1000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company 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

  • CS1000 Light Therapy Device Ref K110558

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

Frequently asked questions

How many devices does Genesis Health Light Corporation have in the registry?

The registry currently lists 1 device for Genesis Health Light Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list Genesis Health Light Corporation's devices?

Among its 1 most recently registered device, Genesis Health Light Corporation has devices listed in FDA 510(k) (1 device).

What risk classes do Genesis Health Light Corporation's devices fall under?

Among its 1 most recently registered device, the classes recorded for Genesis Health Light Corporation's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Genesis Health Light Corporation in the registry?

The most recently registered devices listed for Genesis Health Light Corporation include CS1000 LIGHT THERAPY DEVICE.

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