K Project S.r.l.
IT-MF-000042195 · Italy · Milano
K Project S.r.l. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Devices declared under this manufacturer
- KYMINASI DIET DETOX
- KYMINASI DIET FASE DIETA
- KYMINASI DIET FASE FINALE
- KYMINASI DIET RIPARAZIONE
- KYMINASI DIET SALVADIETA
- KYMINASI DIET STABILIZZAZIONE
- KYMINASI DIET VITALITA'
- KYMINASI VITALITA'
Catalogue references include KDET, KFASE, KFIN, KRIP, KSALV, KSTAB.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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.
North American profile: Neither register. K Project S.r.l. was not found in either the U.S. or the Canadian register.