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Jpi America, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
3

What Jpi America, Inc. makes

Jpi America, Inc. manufactures X-ray equipment including the JPI X-RAY GRID, AJEX 9015/135H PORTABLE X-RAY, and JPI X-RAY FILM CASSETTE.

The company's portfolio consists of Class I and Class II medical devices listed in the FDA 510(k) registry, and it is based in the US.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Jpi X-Ray Grid Ref K945327

    Class I
    Active 510(k) 510(k) I
  • Ajex 9015/135H Portable X-Ray Ref K052341

    Class II
    Active 510(k) 510(k) II
  • Jpi X-Ray Film Cassette Ref K945328

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

Frequently asked questions

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

The registry currently lists 3 devices for Jpi America, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Jpi America, Inc.'s devices?

Among its 3 most recently registered devices, Jpi America, Inc. has devices listed in FDA 510(k) (3 devices).

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

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

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

The most recently registered devices listed for Jpi America, Inc. include JPI X-RAY GRID, AJEX 9015/135H PORTABLE X-RAY and JPI X-RAY FILM CASSETTE.

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