AQUALEG
FR-MF-000004676 · France · THOUARE SUR LOIRE
AQUALEG is registered in the European database on medical devices as a manufacturer, with 151 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 151 |
|---|
Most frequent device types declared: Prosthetic foot.
Devices declared under this manufacturer
- AQUALEG
- QRX ADAPTERS
- SKY FOOT
- SKYFOOT
- SQY FOOT
- SQYFOOT
- TRANSFEMORAL SOFT SHELL PROTECTOR
- TRANSFEMORAL SOFT SHELL PROTECTOR LOWER PART EXTREM COVER
- TRANSFEMORAL SOFT SHELL PROTECTOR SPORT COVER COMPLETE
- TRANSTIBIAL SOFT SHELL PROTECTOR LIGHT COVER
- WAVETIBI001
Showing 12 of 151 declared devices.
Catalogue references include AQ1/2F002, SQYF1A1A1LB2280, SQYF1A1A1LB2310, SQYF1A1A1LB2460, SQYF1A1A1LB2710, SQYF1A1A1RB2410.
European nomenclature codes declared: Y062499, Y062703, Y062409,Y062415.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 151 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 151 |
|---|---|
| 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. AQUALEG was not found in either the U.S. or the Canadian register.