KINVENT Biomecanique
FR-MF-000031884 · France · Montpellier
KINVENT Biomecanique is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 12 |
|---|
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- ECG Electrodes
- K Myo
- K Myo Black
- K Plates Ezygain
- K-Bubble
- K-Deltas
- K-Deltas XL
- K-Force Plates
- K-Grip
- K-Move
- K-Pull
- K-Push
Catalogue references include MP.06.04.FN, MP.08.03.FN, MP.10.02.FN, MP.10.03.FN, MP.27.03.FN, MP.33.03.FN.
European nomenclature codes declared: Z12062601, Z120602, Z12062401, C020501, V030202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | KINVENT BIOMECANIQUE (FR) · FDA 3016566173 |
| Devices in EUDAMED | 12 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| Found in the U.S. device database | 9 |
| Share | 75.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | KINVENT BIOMECANIQUE SAS |
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 1 |
| First licensed | 2024-12-19 |
Licence types: System (1).
Licensed under: K-SENSORS.
North American profile: Both markets. KINVENT Biomecanique is registered in both the United States and Canada.