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Uvx, Inc.

CanadaFDA applicant, unverified

Devices
1

What Uvx, Inc. makes

Uvx, Inc. manufactures the Zener® (model ZEN-001-B1), a device designed for ultraviolet disinfection applications, targeting microbial contamination in medical and environmental settings.

The Zener® 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Zener® (model ZEN-001-B1) Ref K252128

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

Frequently asked questions

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

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

Which registries list Uvx, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Uvx, Inc. include Zener® (model ZEN-001-B1).

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