Footlogics Europe B.V.
NL-MF-000043504 · Netherlands · Almere
Footlogics Europe B.V. is registered in the European database on medical devices as a manufacturer, with 56 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 56 |
|---|
Most frequent device types declared: FOOTLOGICS HIGH HEEL, FOOTLOGICS INSOLE CASUAL, FOOTLOGICS KIDS.
Devices declared under this manufacturer
- FOOTLOGICS CASUAL INSOLE M
- FOOTLOGICS CASUAL INSOLE XL
- FOOTLOGICS COMFORT INSOLE M
- FOOTLOGICS COMFORT INSOLE S
- FOOTLOGICS COMFORT INSOLE XL
- FOOTLOGICS COMFORT PLUS INSOLE S
- FOOTLOGICS COMFORT PLUS INSOLE XL
- FOOTLOGICS HIGH HEEL INSOLE M
- FOOTLOGICS HIGH HEEL INSOLE XS
- FOOTLOGICS SENSI INSOLE L
- FOOTLOGICS SENSI INSOLE M
- FOOTLOGICS SENSI INSOLE XL
Showing 12 of 56 declared devices.
Catalogue references include 1053APS L, 1059MC M, 1069.4SVP S, 1069.4SVP XL, 1069.6VF M, 1069.6VF XS.
European nomenclature codes declared: Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 56 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 56 |
|---|---|
| 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. Footlogics Europe B.V. was not found in either the U.S. or the Canadian register.