LVI Low Vision International AB
SE-MF-000004178 · Sweden · Växjö
LVI Low Vision International AB is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Most frequent device types declared: MAGNI-WIFI, ML-WIFI-CAM, ML-ZIP, ML-iTAB, MLAIR.
Among these devices, 34 are declared active.
Devices declared under this manufacturer
- MAGNI-WIFI
- ML-ITAB-SC-13PRO
- ML-WIFI-CAM
- MLAIR-DUO
- MLPRO-FHD
- MLV-FHD-S27-3V
- MLVBASIC-TTS1
- MLVBASIC-TTS2
- MLVOICE-2
- MLZ-FHD13
- MLZ-FHD13-A
- MLZ-FHD17
Showing 12 of 40 declared devices.
Catalogue references include MAGNI-WIFI, MLPRO, PB-W-Mi, https://lviglobal.se/catalog/products/magnilink-air-duo, https://lviglobal.se/catalog/products/magnilink-voice, https://lviglobal.se/catalog/products/magnilink-wificam.
European nomenclature codes declared: Y210603, Y2199, Y215199, Y210606, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| Country of registration | Sweden |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 40 |
|---|---|
| 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. LVI Low Vision International AB was not found in either the U.S. or the Canadian register.