DOSCA SRL
IT-MF-000031334 · Italy · VOLTA MANTOVANA (MN)
DOSCA SRL is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: Sticktite by OPTXEUROPE.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- Lenti correttive sportive +1.25
- Lenti correttive sportive +1.50
- Lenti correttive sportive +1.75
- Lenti correttive sportive +2.00
- Lenti correttive sportive +2.50
- Lenti correttive sportive +3.00
Catalogue references include 5004, 5011, 5028, 5035, 5042, 5059.
European nomenclature codes declared: Q0210010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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: Neither register. DOSCA SRL was not found in either the U.S. or the Canadian register.