Data / Medical devices / Switzerland / NeuroXtherapeutics SA
NeuroXtherapeutics SA: FDA-registered device maker in Lausanne Vaud, Switzerland, 1 510(k) clearance
NeuroXtherapeutics SA is registered with the FDA (registration 3013517146) in Lausanne Vaud, Switzerland. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 24, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013517146
- Address
- Chemin de Roseneck 5, Lausanne Vaud, Switzerland, 1006
- Owner or operator
- NeuroXtherapeutics SA (10054794)
- Roles
- Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- April 27, 2017
- Registered through
- 2026
- Brand names listed
- Izar, MindMotion Companion, MindMotion GO, MindMotion GO Procedure Pack, MindMotion Pro, MindMotion Toap Run, MindPod Dolphin
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Exerciser, Finger, Powered | JFA | 1 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Interactive Rehabilitation Exercise Device, Prescription Use | QKC | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Interactive Rehabilitation Exercise Devices | LXJ | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 24, 2017 | K162748 | MindMotionPRO | LXJ | Substantially Equivalent | Mindmaze SA | accessdata.fda.gov |
Compare with other makers
- All makers of Exerciser, Finger, Powered
- All makers of Interactive Rehabilitation Exercise Devices
- All makers of Interactive Rehabilitation Exercise Device, Prescription Use
Updated April 24, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.