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Nagata Engineering Co.

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Devices
1

What Nagata Engineering Co. makes

Nagata Engineering Co. manufactures the NEURO PULSE II, a medical device designed for neurological monitoring or stimulation applications.

The NEURO PULSE II is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. 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

  • Neuro Pulse Ii Ref K853836

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

Frequently asked questions

How many devices does Nagata Engineering Co. have in the registry?

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

Which registries list Nagata Engineering Co.'s devices?

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

What risk classes do Nagata Engineering Co.'s devices fall under?

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

What are the newest devices from Nagata Engineering Co. in the registry?

The most recently registered devices listed for Nagata Engineering Co. include NEURO PULSE II.

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