Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043014934

FEI Number

3043014934

Entity Name

NAOX TECHNOLOGIES SAS

City/State/Country

Paris Ile-de-France, FR

Establishment Address

62 rue mazarine, Paris Ile-de-France 75006, FR

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

NAOX TECHNOLOGIES (Owner Number: 10094901)

Owner / Operator Contact Address

73 rue Leon Bourgeois, Palaiseau, FR-91 91120, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K251550

PMA Number

N/A

All Registered Proprietary Names

Naox Link

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OMC	Reduced- Montage Standard Electroencephalograph	Neurology	Class 2	882.1400	2026-01-05

Official Correspondent

Stephane Mazet

US Agent Details

Scott Bednar Business: QA/RA CONSULTING GROUP, INC. Email: sbednar@qaraconsultinggroup.com Phone: (412) 4188066

Related Public Records

Same Entity

NAOX TECHNOLOGIES

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043014934. Last updated year: 2026. Please use registration number 3043014934 when referencing this establishment in official correspondence.