Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1121806

FEI Number

1121806

Entity Name

Neurotron Inc

City/State/Country

Aurora, CO, US

Establishment Address

12635 East Montview Blvd, Suite 127, Aurora, CO 80045, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Neurotron, Inc (Owner Number: 1121806)

Owner / Operator Contact Address

6637 charlesway, --, Towson, MD 21204, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CBEX Electrode Cable

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKD	Cable, Electrode	Physical Medicine	Class 2	890.1175	1992-12-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neurotron, Inc

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 1121806. Last updated year: 2026. Please use registration number 1121806 when referencing this establishment in official correspondence.