Reingenuity Ltd
UK-MF-000052788 · United Kingdom · Lincolnshire
Reingenuity Ltd is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Among these devices, 3 are declared sterile.
Authorised representative in the Union: Eurolink Europe Compliance Limited.
Devices declared under this manufacturer
- Culture+
- Honan Balloon
- Justfix+
- Paradevice
Showing 12 of 18 declared devices.
Catalogue references include 107-007, 110-007, 210, 500, 700-007, 707-007.
European nomenclature codes declared: W050301020101, L1799, W050301020102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | REINGENUITY (US) · FDA 3040602660 |
| Devices in EUDAMED | 18 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 18 |
|---|---|
| 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. Reingenuity Ltd is registered in the United States but was not found in the Canadian register.