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Anrad Corp.

United StatesFDA applicant, unverified

Devices
2

What Anrad Corp. makes

Anrad Corp. manufactures digital radiation detectors, including the GR17 Digital Detector, designed for use in medical imaging systems to capture X-ray images for diagnostic purposes.

The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • GR17 Digital Detector Ref K052136

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Digital Detector, Model GR17 Ref K042821

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

Frequently asked questions

How many devices does Anrad Corp. have in the registry?

The registry currently lists 2 devices for Anrad Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Anrad Corp.'s devices?

Among its 2 most recently registered devices, Anrad Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Anrad Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Anrad Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Anrad Corp. in the registry?

The most recently registered devices listed for Anrad Corp. include GR17 DIGITAL DETECTOR and DIGITAL DETECTOR, MODEL GR17.

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