NeuroX USA Inc

FDA Device Registration & Listing · Raleigh, NC, US · Registration 3044679953

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3044679953
FEI Number
3044679953
Entity Name
NeuroX USA Inc
City/State/Country
Raleigh, NC, US
Establishment Address
3915 Beryl Rd Ste 120, Raleigh, NC 27607, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
NeuroXtherapeutics SA (Owner Number: 10054794)
Owner / Operator Contact Address
Chemin de Roseneck 5, Lausanne, CH-VD 1006, CH
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MindMotion GO MindPod Dolphin MindMotion Toap Run MindMotion GO Procedure Pack

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKC Interactive Rehabilitation Exercise Device, Prescription Use Physical Medicine Class 2 890.5360 2022-01-27

Official Correspondent

Pomme Boissier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeuroXtherapeutics SA
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3013517146 NeuroXtherapeutics SA Lausanne Vaud, CH

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044679953. Last updated year: 2026. Please use registration number 3044679953 when referencing this establishment in official correspondence.
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