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Fujitsu, Ltd.

Country not established

Devices
1

What Fujitsu, Ltd. makes

Fujitsu, Ltd. manufactures the INFRA-EYE 160 device, which is a Class I medical device.

The device is listed in the FDA 510(k) registry, and the company is based in the US.

AI-generated from registry data, 21 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Infra-Eye 160 Ref K841271

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Fujitsu, Ltd. have in the registry?

The registry currently lists 1 device for Fujitsu, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Fujitsu, Ltd.'s devices?

Among its 1 most recently registered device, Fujitsu, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Fujitsu, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Fujitsu, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Fujitsu, Ltd. in the registry?

The most recently registered devices listed for Fujitsu, Ltd. include INFRA-EYE 160.

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