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Icm Co., Ltd.

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Devices
1

What Icm Co., Ltd. makes

Icm Co., Ltd. manufactures the UBIPACS, a medical device designed for use in specific diagnostic or monitoring applications within the cardiovascular field.

The UBIPACS is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. 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

  • Ubipacs Ref K042507

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

Frequently asked questions

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

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

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

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

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

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

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

The most recently registered devices listed for Icm Co., Ltd. include UBIPACS.

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