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Robert Gold Assoc.

Country not established

Devices
1

What Robert Gold Assoc. makes

Robert Gold Assoc. manufactures the AIR-MEDEX I, a medical device designed for respiratory support and ventilation purposes, likely used in clinical or emergency settings to assist patients with breathing.

The AIR-MEDEX I 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Air-Medex I Ref K961769

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

Frequently asked questions

How many devices does Robert Gold Assoc. have in the registry?

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

Which registries list Robert Gold Assoc.'s devices?

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

What risk classes do Robert Gold Assoc.'s devices fall under?

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

What are the newest devices from Robert Gold Assoc. in the registry?

The most recently registered devices listed for Robert Gold Assoc. include AIR-MEDEX I.

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