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X-Ray Tube Corp.

United StatesFDA 510(k) applicant, unverified

Devices
3

What X-Ray Tube Corp. makes

X-Ray Tube Corp. manufactures CRISA X-ray tubes, which are designed for use in diagnostic imaging systems.

These devices are classified as Class I under FDA regulations and are 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.

Catalogue3

Newest first, rows 1-3 of 3

  • Crisa Ref K840135

    Class I
    Active 510(k) 510(k) I

  • Crisa Ref K833238

    Class I
    Active 510(k) 510(k) I

  • Crisa Ref K833847

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does X-Ray Tube Corp. have in the registry?

The registry currently lists 3 devices for X-Ray Tube Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list X-Ray Tube Corp.'s devices?

Among its 3 most recently registered devices, X-Ray Tube Corp. has devices listed in FDA 510(k) (3 devices).

What risk classes do X-Ray Tube Corp.'s devices fall under?

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

What are the newest devices from X-Ray Tube Corp. in the registry?

The most recently registered devices listed for X-Ray Tube Corp. include CRISA.

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