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 IIa | 298 |
|---|
Most frequent device types declared: 131S, 139S, 302XS, 721S, 723S.
Authorised representative in the Union: European Healthcare & Device Solutions Ltd..
Catalogue references include 131, 302, 723, 754, 762, 895K.
European nomenclature codes declared: Y061209, Y06120601, Y061203, M030405, Y060399, Y060609.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NEO G LIMITED (GB) · FDA 3010453133 |
| Devices in EUDAMED | 298 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 298 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. Neo G Limited is registered in the United States but was not found in the Canadian register.