LA MAISON DENTAIRE SA
LI-MF-000004625 · Liechtenstein · BALZERS
LA MAISON DENTAIRE SA is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: FINTREC MATRICI ACCIAIO, FINTREC MATRICI TRASPARENTI, MEDI KORD A.S. 9, SPLINT MAT NYLON.
Devices declared under this manufacturer
- Asba Flour Prophy Paste
- Asba Fluor Gel
- FINTREC MATRICI ACCIAIO
- FINTREC MATRICI TRASPARENTI
- FLEXIBLE SCALER
- Impresil
- MEDI KORD A.S. 9
- PERFOMAT
- SPLINT MAT NYLON
Catalogue references include 1002, 1658, 265, 266, 268, 436.
European nomenclature codes declared: Q01010401, Q010199, Q010204.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | La Maison Dentaire / Medirel SA (CH) · FDA 3009488939 |
| Devices in EUDAMED | 9 |
| Country of registration | Liechtenstein |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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.