LABORATOIRES VIVACY
FR-MF-000003771 · France · ARCHAMPS
LABORATOIRES VIVACY is registered in the European database on medical devices as a manufacturer, with 118 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 118 |
|---|
Most frequent device types declared: DESIRIAL®, INTRA ARTICULAR, STYLAGE ® LIDOCAINE, STYLAGE®, STYLAGE® LIDOCAINE.
Among these devices, 118 are declared sterile, 118 implantable.
Catalogue references include SPF099, SPF238, SPF253, SPF257, SPF531, SPF543.
European nomenclature codes declared: X0303, P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 118 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 81 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | LABORATOIRES VIVACY |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 3 devices | 3 |
| First licensed | 2015-08-27 |
Licence types: Device Group Family (1), System (1), Device Group (1).
Licensed under: STYLAGE, STYLAGE XXL (VOLUMIZERS), STYLAGE XL LIDOCAINE.
North American profile: Canada only. LABORATOIRES VIVACY holds a Canadian licence but was not found in the U.S. register.