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Hinnovation, Inc.

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Devices
1

What Hinnovation, Inc. makes

Hinnovation, Inc. manufactures the ICONNECTION 3D, a Class II medical device designed for three-dimensional imaging or connectivity applications in clinical settings.

The ICONNECTION 3D is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. 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

  • Iconnection 3D Ref K012779

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

Frequently asked questions

How many devices does Hinnovation, Inc. have in the registry?

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

Which registries list Hinnovation, Inc.'s devices?

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

What risk classes do Hinnovation, Inc.'s devices fall under?

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

What are the newest devices from Hinnovation, Inc. in the registry?

The most recently registered devices listed for Hinnovation, Inc. include ICONNECTION 3D.

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