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Vivaray, Inc.

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Devices
1

What Vivaray, Inc. makes

Vivaray, Inc. manufactures the CAPRI Applicator, a device designed for transdermal drug delivery applications, facilitating precise administration of medications through the skin.

The CAPRI Applicator is classified as a Class II medical device in the United States and is listed under the FDA’s 510(k) pathway. The company is based in the US.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Capri Applicator Ref K092822

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

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

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

Which registries list Vivaray, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Vivaray, Inc. include CAPRI APPLICATOR.

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