Mosaic Surgical Ltd
GB-MF-000003512 · United Kingdom · High Wycombe
Mosaic Surgical Ltd is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 63 |
|---|
Most frequent device types declared: JUNE3000, JUNE3000B12, JUNE3000S5, JUNE3000SB5, JUNE3001B5.
Among these devices, 62 are declared sterile.
Authorised representative in the Union: JUNE Medical Sverige AB.
Devices declared under this manufacturer
- Galaxy II
- Galaxy II Surgical Retractor
- eVeck
Showing 12 of 63 declared devices.
Catalogue references include JUNE3000B12, JUNE3000S5, JUNE3000SB5, JUNE3001B5, JUNE3002S-8, JUNEGX-2020.
European nomenclature codes declared: K01020106, L03140101, K01020112, L03140104, L03140199, K01020114.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MOSAIC SURGICAL (GB) · FDA 3016170849 |
| Devices in EUDAMED | 63 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 61 |
|---|---|
| Found in the U.S. device database | 60 |
| Share | 98.4 % |
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. Mosaic Surgical Ltd is registered in the United States but was not found in the Canadian register.