Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013263129

FEI Number

3013263129

Entity Name

2BREATHE TECHNOLOGIES LTD

City/State/Country

Raanana Central, IL

Establishment Address

16 Hatidhar St., Raanana Central 43652, IL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

2breathe technologies LTD (Owner Number: 10052413)

Owner / Operator Contact Address

16 Hatidhar St., Raanana, IL-NOTA 43652, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K020399

PMA Number

N/A

All Registered Proprietary Names

RESPeRATE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2016-07-25

Official Correspondent

George Hattub

US Agent Details

George Hattub Business: Medicsense USA Email: ghattub@comcast.net Phone: (508) 4796116

Related Public Records

Same Entity

2breathe technologies 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
3004642067	NEUROCONN GMBH	Ilmenau Thuringia, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013263129. Last updated year: 2026. Please use registration number 3013263129 when referencing this establishment in official correspondence.