UAB Kavita
LT-MF-000002717 · Lithuania · Mažeikiai
UAB Kavita is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: EXFASH EYEWEAR, KID, Lenny Lance New York, OP CHART Mišrios dešimtainės, RB-266.
Devices declared under this manufacturer
- Bandomieji rėmeliai
- Bandomųjų lešių rėmelis
- Bandomųjų lęšių rinkinys
- EXFASH
- Lenny Lance NEW YORK
- Švieslentė regėjimo aštrumui nustatyti \
Catalogue references include KID/56, MA L21047/01, MV1412 EF4561/203, OP CHART, RB-266CM COLORED, RB-301.
European nomenclature codes declared: Q0299, Q02100299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Lithuania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| 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. UAB Kavita was not found in either the U.S. or the Canadian register.