Skip to content

Intex Research & Development Center

Country not established

Devices
1

What Intex Research & Development Center makes

Intex Research & Development Center manufactures the ALEXIS device, which is classified as a Class II medical device.

The company is based in the US and the ALEXIS device is listed in the FDA 510(k) registry.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Alexis Ref K851261

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

Frequently asked questions

How many devices does Intex Research & Development Center have in the registry?

The registry currently lists 1 device for Intex Research & Development Center. Devices recorded under merged duplicate company entries are counted once.

Which registries list Intex Research & Development Center's devices?

Among its 1 most recently registered device, Intex Research & Development Center has devices listed in FDA 510(k) (1 device).

What risk classes do Intex Research & Development Center's devices fall under?

Among its 1 most recently registered device, the classes recorded for Intex Research & Development Center's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Intex Research & Development Center in the registry?

The most recently registered devices listed for Intex Research & Development Center include ALEXIS.

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