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Mallinckrodt Group, Inc.

United StatesFDA applicant, unverified

Devices
27

What Mallinckrodt Group, Inc. makes

The company manufactures radiographic imaging accessories and systems, including X-ray film conveyance solutions, automatic cassette loaders, and flexible grid cassettes for digital imaging. It also produces urological tables for intravenous procedures, coiled extension tubing for medical lines, and contrast injection systems for computed tomography (CT) and angiography, such as the Angiomat CT Injector and CT 8000 Digital Injection System. Additional offerings include radiographic X-ray systems for neurosurgery and urological imaging devices like the Uro-Flo.

The portfolio includes devices classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance database. These products are intended for use in radiography, urology, and CT imaging procedures. The company is headquartered in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Mallinckrodt Group, Inc. have in the registry?

The registry currently lists 27 devices for Mallinckrodt Group, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mallinckrodt Group, Inc.'s devices?

Among its 27 most recently registered devices, Mallinckrodt Group, Inc. has devices listed in FDA 510(k) (27 devices).

What risk classes do Mallinckrodt Group, Inc.'s devices fall under?

Among its 27 most recently registered devices, the classes recorded for Mallinckrodt Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mallinckrodt Group, Inc. in the registry?

The most recently registered devices listed for Mallinckrodt Group, Inc. include ANGIOMAT 6000, AUTOMATIC CASSETTE LOADER, X-RAY FILM, CONVEY OR SYSTEM and HYDRAJUST IV UROLOGICAL TABLE.

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