Polydentia SA
CH-MF-000008779 · Switzerland · Mezzovico-Vira
Polydentia SA is registered in the European database on medical devices as a manufacturer, with 402 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 402 |
|---|
Most frequent device types declared: Dental Abrasives - ASTIDENTAL, Dental matrices - LIFCO, Forceps SwissMat, Metal matrices - ASTIDENTAL, Plastic matrices - ASTIDENTAL.
Authorised representative in the Union: IDD International Dental Distributors AG.
Devices declared under this manufacturer
- Lumicontrast sectional matrices
- Prodonto MATRIXMART Linea Matrici
- Prodonto MATRIXMART Linea matrici
- Prodonto Strip abrasiva
- Quickmat Silicone tubes
- Quickmat quickrings
- QuickmatFLEX sectional matrices
- Roeko-Strip
- Simplee Molar + Extension Sectional Matrix Bands
- Strip ST
- Strip soft
- contoured anatomical matrices
Showing 12 of 402 declared devices.
Catalogue references include 5507, 5710, 5711, 6766, PROB40003MM7, PROB40005MM6.
European nomenclature codes declared: Q01010401, Q010199, Q01010199, Q01010403, Q01010104.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | POLYDENTIA S.A. (CH) · FDA 8031054 |
| Devices in EUDAMED | 402 |
| Country of registration | Switzerland |
⚠️ A similar name exists; we do not assert it is the same company — why.
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.