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Vitajet Corp.

United StatesFDA applicant, unverified

Devices
3

What Vitajet Corp. makes

Vitajet Corp. makes the VITAJET, MEDIVAX, and VITAPEN devices.

These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Vitajet Ref K962625

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Medivax Ref K945548

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Vitapen Ref K924447

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

Frequently asked questions

How many devices does Vitajet Corp. have in the registry?

The registry currently lists 3 devices for Vitajet Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vitajet Corp.'s devices?

Among its 3 most recently registered devices, Vitajet Corp. has devices listed in FDA 510(k) (3 devices).

What risk classes do Vitajet Corp.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Vitajet Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vitajet Corp. in the registry?

The most recently registered devices listed for Vitajet Corp. include VITAJET, MEDIVAX and VITAPEN.

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