Pixee Medical
FR-MF-000001534 · France · Besancon
Pixee Medical is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: Orthopedic Instrument.
Among these devices, 1 are declared reusable, 4 active, 4 with a measuring function.
Devices declared under this manufacturer
- KneePlus 1.6
- KneePlus v1.7
- Pointer
- ShoulderPlus 1.1
Catalogue references include KCS170, KNI001, KNS160, KNS170, SHS110.
European nomenclature codes declared: Z12130482, Z12130480.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PIXEE MEDICAL (FR) · FDA 3020703212 |
| Devices in EUDAMED | 5 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 3 |
| Share | 60.0 % |
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. Pixee Medical is registered in the United States but was not found in the Canadian register.