Skip to content

Discovery Engineering Intl., Inc.

Country not established

Devices
1

What Discovery Engineering Intl., Inc. makes

Discovery Engineering Intl., Inc. manufactures the DEI Model 20 EEG device.

The DEI Model 20 EEG is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Dei Model 20 Eeg Ref K961718

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

Frequently asked questions

How many devices does Discovery Engineering Intl., Inc. have in the registry?

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

Which registries list Discovery Engineering Intl., Inc.'s devices?

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

What risk classes do Discovery Engineering Intl., Inc.'s devices fall under?

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

What are the newest devices from Discovery Engineering Intl., Inc. in the registry?

The most recently registered devices listed for Discovery Engineering Intl., Inc. include DEI MODEL 20 EEG.

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