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Mediface Co., Ltd.

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Devices
1

What Mediface Co., Ltd. makes

Mediface Co., Ltd. manufactures a Picture Archiving and Communication System (PACS), a digital network used for storing, retrieving, and displaying medical images and reports for diagnostic and treatment purposes.

The company’s PACS system is classified as a Class II medical device under FDA regulations and is listed via the 510(k) premarket notification process. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Mediface Pacs Ref K010259

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

Frequently asked questions

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

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

Which registries list Mediface Co., Ltd.'s devices?

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

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

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

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

The most recently registered devices listed for Mediface Co., Ltd. include MEDIFACE PACS.

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