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Transverse Industries Co.

TaiwanFDA applicant, unverified

Devices
1

What Transverse Industries Co. makes

Transverse Industries Co. makes a skin care light device.

The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Skin Care Light Ref K070870

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

Frequently asked questions

How many devices does Transverse Industries Co. have in the registry?

The registry currently lists 1 device for Transverse Industries Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Transverse Industries Co.'s devices?

Among its 1 most recently registered device, Transverse Industries Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Transverse Industries Co.'s devices fall under?

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

What are the newest devices from Transverse Industries Co. in the registry?

The most recently registered devices listed for Transverse Industries Co. include SKIN CARE LIGHT.

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