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A & D Corporate

Country not established

Devices
1

What A & D Corporate makes

A & D Corporate manufactures the A&D UN-231 Ultrasonic Handy Nebulizer, a portable device designed for delivering aerosolized medication via inhalation therapy.

The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer 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

Frequently asked questions

How many devices does A & D Corporate have in the registry?

The registry currently lists 1 device for A & D Corporate. Devices recorded under merged duplicate company entries are counted once.

Which registries list A & D Corporate's devices?

Among its 1 most recently registered device, A & D Corporate has devices listed in FDA 510(k) (1 device).

What risk classes do A & D Corporate's devices fall under?

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

What are the newest devices from A & D Corporate in the registry?

The most recently registered devices listed for A & D Corporate include A&D UN-231 ULTRASONIC HANDY NEBULIZER.

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