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G-Medical Innovations, Ltd.

IsraelFDA 510(k) applicant, unverified

Devices
2

What G-Medical Innovations, Ltd. makes

G-Medical Innovations, Ltd. manufactures the Prizma, a medical device designed for diagnostic imaging and analysis, likely used in radiology or laboratory settings to process and evaluate blood samples or other biological specimens.

The company’s portfolio is regulated under Class II devices in the United States, with individual products authorised through the FDA’s 510(k) clearance process. The manufacturer is based in the US.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Prizma Ref K173589

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

  • Prizma Ref K170181

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

Frequently asked questions

How many devices does G-Medical Innovations, Ltd. have in the registry?

The registry currently lists 2 devices for G-Medical Innovations, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list G-Medical Innovations, Ltd.'s devices?

Among its 2 most recently registered devices, G-Medical Innovations, Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do G-Medical Innovations, Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for G-Medical Innovations, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from G-Medical Innovations, Ltd. in the registry?

The most recently registered devices listed for G-Medical Innovations, Ltd. include Prizma.

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