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General Electric Co.

Also registered as GENERAL ELECTRIC COMPANY, Intl. General Electric Co.

Country not established

Devices
257

What General Electric Co. makes

The company manufactures diagnostic imaging equipment, including high-voltage X-ray generators, computed tomography (CT) scanners, ultrasound systems, and fluoroscopy components. Their portfolio also includes film processors, diagnostic workstations, and information management systems for radiology and cardiology. Rectal probe covers and specialized suspension hardware for imaging devices are also produced.

These devices are regulated under FDA classifications, with most falling under Class I or Class II. They appear in the FDA’s 510(k) and PMA clearance records, indicating compliance with U.S. medical device regulations. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue257

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Frequently asked questions

How many devices does General Electric Co. have in the registry?

The registry currently lists 257 devices for General Electric Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list General Electric Co.'s devices?

Among its 50 most recently registered devices, General Electric Co. has devices listed in FDA 510(k) (50 devices).

What risk classes do General Electric Co.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for General Electric Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from General Electric Co. in the registry?

The most recently registered devices listed for General Electric Co. include GENERATOR, HIGH VOLT, X-RAY, DIAG. MPX80, SENOGRAPH DS, SENOGRAPH ESSENSTIAL, SENOGRAPHE DS, SENOGRAPHE ESSENTIAL and GE CT/T 8800 SYSTEM.

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