DENTAL MANUFACTURING S.P.A
IT-MF-000027222 · Italy · BADIA POLESINE (RO)
DENTAL MANUFACTURING S.P.A is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: 0720002, 2040003.
Devices declared under this manufacturer
- ACRY TRAY LIQ. 250 ML
- ACRY TRAY LIQ. 500 ML
- ACRY TRAY POLV. 1000 GR.
- ACRY TRAY POLV. 500 GR.
- ACRY TRAY POLV. 5000 GR.
- ALGINATO CROMATICO 450 GR.
- ALGINATO DUST FREE 450 GR.
Catalogue references include 0720002, 0730002, 0750002, 0760002, 0780002, 2040003.
European nomenclature codes declared: Q01020199, Q01020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | DENTAL MANUFACTURING S.P.A. |
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 1 |
| First licensed | 2011-07-26 |
Licence types: Device Family (1).
Licensed under: ARTIFICIAL ACRYLIC TEETH.
North American profile: Canada only. DENTAL MANUFACTURING S.P.A holds a Canadian licence but was not found in the U.S. register.