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Digital Imaging Co. of America

Country not established

Devices
1

What Digital Imaging Co. of America makes

Digital Imaging Co. of America manufactures the CAMTEX 1000, a medical imaging device designed for diagnostic imaging purposes, likely within radiology or fluoroscopy applications.

The CAMTEX 1000 is classified as a Class II device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Camtex 1000 Ref K840134

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Digital Imaging Co. of America have in the registry?

The registry currently lists 1 device for Digital Imaging Co. of America. Devices recorded under merged duplicate company entries are counted once.

Which registries list Digital Imaging Co. of America's devices?

Among its 1 most recently registered device, Digital Imaging Co. of America has devices listed in FDA 510(k) (1 device).

What risk classes do Digital Imaging Co. of America's devices fall under?

Among its 1 most recently registered device, the classes recorded for Digital Imaging Co. of America's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Digital Imaging Co. of America in the registry?

The most recently registered devices listed for Digital Imaging Co. of America include CAMTEX 1000.

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