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Shima American Corp.

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Devices
1

What Shima American Corp. makes

Shima American Corp. manufactures the SANKEN MAT, a medical device designed for patient positioning and support in surgical and clinical settings, ensuring stability and alignment during procedures.

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

  • Sanken Mat Ref K924005

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

Frequently asked questions

How many devices does Shima American Corp. have in the registry?

The registry currently lists 1 device for Shima American Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shima American Corp.'s devices?

Among its 1 most recently registered device, Shima American Corp. has devices listed in FDA 510(k) (1 device).

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

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

What are the newest devices from Shima American Corp. in the registry?

The most recently registered devices listed for Shima American Corp. include SANKEN MAT.

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