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Lexicor

Country not established

Devices
1

What Lexicor makes

Lexicor makes medical devices such as the NEUROSEARCH-4, which is a type of device used for neurological purposes.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 23 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Neurosearch-4 Ref K920038

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

Frequently asked questions

How many devices does Lexicor have in the registry?

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

Which registries list Lexicor's devices?

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

What risk classes do Lexicor's devices fall under?

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

What are the newest devices from Lexicor in the registry?

The most recently registered devices listed for Lexicor include NEUROSEARCH-4.

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