KineQuantum
FR-MF-000024566 · France · Saint-Mandé
KineQuantum is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 28 |
|---|
Most frequent device types declared: KQSOFT, KQSOFTHOME, KQSTRAP.
Among these devices, 24 are declared active.
Devices declared under this manufacturer
- KineQuantum Liberty
- KineQuantum Premium
- KineQuantum Pro
- KineQuantum Wireless
- KineQuantum éco
- Shoulder Straps
- Straps L
- Straps M
- Straps S
Showing 12 of 28 declared devices.
Catalogue references include 20103, 20104, 20107, 20206, 20404, 21406.
European nomenclature codes declared: Z12069099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. KineQuantum was not found in either the U.S. or the Canadian register.