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Selex, Inc.

Country not established

Devices
1

What Selex, Inc. makes

Selex, Inc. manufactures the Polarex and Polarex MLD, which are medical devices designed for electrotherapy applications, likely targeting muscle stimulation or pain management through electrical impulses.

These devices fall under Class I regulation in the US, with the Polarex and Polarex MLD listed via the FDA’s 510(k) pathway. 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

  • Polarex And Polarex Mld Ref K863651

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

Frequently asked questions

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

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

Which registries list Selex, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Selex, Inc. include POLAREX AND POLAREX MLD.

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