Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017773925

FEI Number

3017773925

Entity Name

NEUROTRACK TECHNOLOGIES

City/State/Country

Redwood City, CA, US

Establishment Address

303 Twin Dolphin Dr., Suite 600, Redwood City, CA 94065, US

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Neurotrack Technologies (Owner Number: 10079206)

Owner / Operator Contact Address

303 Twin Dolphin Dr., Suite 600, Redwood City, CA 94065, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Neurotrack Cognitive Assessment Battery

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PTY	Computerized Cognitive Assessment Aid, Exempt	Neurology	Class 2	882.1470	2020-11-23

Official Correspondent

Katie Wallace

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neurotrack 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 3017773925. Last updated year: 2026. Please use registration number 3017773925 when referencing this establishment in official correspondence.