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Inet Corp.

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Devices
1

What Inet Corp. makes

Inet Corp. manufactures the INET Model Biovision, a Class II medical device designed for imaging-based diagnostic applications, likely supporting real-time or stored visual analysis in clinical settings.

The INET Model Biovision is regulated under the US 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Inet Model Biovision Ref K873834

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

Frequently asked questions

How many devices does Inet Corp. have in the registry?

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

Which registries list Inet Corp.'s devices?

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

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

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

What are the newest devices from Inet Corp. in the registry?

The most recently registered devices listed for Inet Corp. include INET MODEL BIOVISION.

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