MEDLAC S.r.l.
IT-MF-000030386 · Italy · AVELLINO (AV)
MEDLAC S.r.l. is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Most frequent device types declared: OK NIGHT.
Catalogue references include MED CUSTOM OK, OK NIGHT (DBR), OK NIGHT (GOV), OK NIGHT (TOP), OK NIGHT (TR), OK NIGHT BI-TORIC.
European nomenclature codes declared: Q02100499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 19 |
|---|---|
| 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. MEDLAC S.r.l. was not found in either the U.S. or the Canadian register.