Hocoma AG
CH-MF-000014672 · Switzerland · Volketswil
Hocoma AG is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|
Among these devices, 35 are declared active.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- ArmeoSpring
- ArmeoSpring Pediatric
- ErigoPro
- LokomatPro L6.2 AD 220V
- Lokomat®Pro 6.3 AD
- Lokomat®Pro 6.3 AD Motivation
- Lokomat®Pro 6.3 Kombi
- Lokomat®Pro 6.3 PE Motivation
- Lokomat®Pro L6.2 AD 120V
- Lokomat®Pro L6.2 FD AD 110V
- Lokomat®Pro L6.2 FD Kombi 110V
- Lokomat®Pro L6.2 FD Kombi 220V
Showing 12 of 37 declared devices.
Catalogue references include 29565, 30000, 30681, 32001, 63055, 63056.
European nomenclature codes declared: N010299, N01028099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 37 |
|---|---|
| Found in the U.S. device database | 36 |
| Share | 97.3 % |
⚠ The two levels disagree here. This company’s name was not found in the FDA establishment register, yet some of its devices are in the U.S. device database. The likeliest reading is that the name match failed.
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | HOCOMA AG |
North American profile: Canada only. Hocoma AG holds a Canadian licence but was not found in the U.S. register.