Pletra Ltd.
LT-MF-000004741 · Lithuania · Kaunas
Pletra Ltd. is registered in the European database on medical devices as a manufacturer, with 167 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 167 |
|---|
Most frequent device types declared: Silicone Foot Orthotic Devices (Footcare).
Devices declared under this manufacturer
- GUOSTE
- GUOSTĖ
Showing 12 of 167 declared devices.
Catalogue references include Heart E-3,5, Left C-4,5, Left C-6,5, Oval A-5, Right D-12, Triangle F-12.
European nomenclature codes declared: Y063018, Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 167 |
| 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 | 167 |
|---|---|
| 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. Pletra Ltd. was not found in either the U.S. or the Canadian register.