Larident SRL
IT-MF-000007807 · Italy · GENOVA (Tribogna)
Larident SRL is registered in the European database on medical devices as a manufacturer, with 224 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 224 |
|---|
Devices declared under this manufacturer
- 2 Cheek retractors
- Arco diga in plastica
- Composite brushes
- Endo Box
- Endo Sponges
- Endodontic ruler set
- Endodontic sponges
- Handle for composite brushes
- Mixing Pad | Foil
- Porta impronte in metallo
- Porta spugnette per endodonzia
- Portaimpronta monouso in pvc
Showing 12 of 224 declared devices.
Catalogue references include C33-D.F., G29.VERDE, MA0INF, ML2SUP, MR1, MT-3SUP 6pz.
European nomenclature codes declared: Q010207, Q010199, Q0199, Q019006, A13, L150201.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LARIDENT S.R.L. (IT) · FDA 9680507 |
| Devices in EUDAMED | 224 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 224 |
|---|---|
| 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.