Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029923663

FEI Number

3029923663

Entity Name

I-BRAINTECH LTD

City/State/Country

Tel Aviv-Yafo, IL

Establishment Address

30, Ibn Gabirol, St, Tel Aviv-Yafo 6407807, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

i-BrainTech LTD (Owner Number: 10088971)

Owner / Operator Contact Address

Beit Tsuri Eliyahu 30-13, Tel Aviv, IL-TA 6912229, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

iBrainTech i-BrainTech i-Brain iBrain

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2023-10-26

Official Correspondent

Konstantin Sonkin

US Agent Details

Mateo Carrasco Business: REGULATORY PHARMA WORLD LLC Email: mateo@afpharmaservice.com Phone: (689) 2471190

Related Public Records

Same Entity

i-BrainTech LTD

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

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3038620647	KISO EHF	Reykjavik, IS
3005196642	HARMONIC ENERGETIC TECHNOLOGIES, LLC	Liverpool, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029923663. Last updated year: 2026. Please use registration number 3029923663 when referencing this establishment in official correspondence.