DMP Dental Industry S.A.
GR-MF-000019283 · Greece · Attiki
DMP Dental Industry S.A. is registered in the European database on medical devices as a manufacturer, with 1 054 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 1 054 |
|---|
Among these devices, 741 are declared implantable.
Devices declared under this manufacturer
- Bona-Bite Air (SFS) 50ml x 2
- Bona-Bite Air (SFS) Chocomint 50ml x 2 - starter pack
- Bonascan Putty (RS) 400g+400g
- Bonasil A+ Regular (RS) 50ml x 2 - starter pack
- Bright Flow Core DC 5ml x 50 syr. Blue
- Bright Light 1.5kg A3
- Bright Light Flow 2g x 4 - G
- Bright Light Flow 2g x 50 Opaque A2
- Bright Posterior 0.25g x 20 A2
- Bright Posterior 4g x 4 - V
- Bright Temporary C&B 1:1 5ml/7.5g B1
- Bright Temporary C&B 4:1 50ml C2
Showing 12 of 1 054 declared devices.
Catalogue references include 120120107, 120120312, 140112707, 150112418C, 180122502, 210105011.
European nomenclature codes declared: Q01010103, Q01020102, Q01020605, Q01010104, Q01010402, Q010499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DMP Dental Industry S.A. (GR) · FDA 3008966075 |
| Devices in EUDAMED | 1 054 |
| Country of registration | Greece |
Device-level evidence
| Devices with a numeric GTIN | 1 054 |
|---|---|
| Found in the U.S. device database | 258 |
| Share | 24.5 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | DMP DENTAL INDUSTRY SA. |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 6 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 2 |
| Class 3 devices | 4 |
| First licensed | 2020-05-29 |
Licence types: Device Family (4), Device Group Family (2).
Licensed under: ETCHING GEL, BRIGHT TEMPORARY C&B, BRIGHT (LIGHT CURING COMPOSITES), BRIGHT FLOW CORE, PIT & FISSURE SEALANT, BRIGHT CAVITY LINER.