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Neo G Limited

GB-MF-000004603 · United Kingdom · Knaresborough

Neo G Limited is registered in the European database on medical devices as a manufacturer, with 298 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa298

Most frequent device types declared: 130SA, 920S-B, 930S-B, 970S-B, 724S.

Authorised representative in the Union: IE-AR-000003999.

United States market access

FDA establishment registerRegistered with FDA
Matched entryNEO G LIMITED (GB) · FDA 3010453133
Devices in EUDAMED298
Country of registrationUnited Kingdom

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