Hopper
FR-MF-000024280 · France · Albi
Hopper is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 27 |
|---|
Devices declared under this manufacturer
- Audacieuse by Hopper L
- Audacieuse by Hopper XL
- Audacieuse by Hopper XS
- Intrepide by Hopper PM
- Intrepide by Hopper PS
- Outsider by Hopper TM-A
- Outsider by Hopper TS-A
- Outsider by Hopper TS-B
- Outsider by Hopper TXL-B
- Outsider by Hopper TXS-A
- Outsider by Hopper TXS-B
- Salomon Footshell multiaxial upper and heel pads Sh1
Showing 12 of 27 declared devices.
Catalogue references include HL01L, HL01XS, HL01XXL, HL02PS, HM02-2, HP01TM-A.
European nomenclature codes declared: Y062499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HOPPER (FR) · FDA 3033557295 |
| Devices in EUDAMED | 27 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 27 |
|---|---|
| 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: United States only. Hopper is registered in the United States but was not found in the Canadian register.