Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038185754

FEI Number

3038185754

Entity Name

AGADO LIVE LTD.

City/State/Country

Bnei Brak Central, IL

Establishment Address

5 Hayarkon st, Bnei Brak Central 5120156, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Agado Live Ltd. (Owner Number: 10092943)

Owner / Operator Contact Address

5 Hayarkon st, Bnei Brak, IS-11 5120156, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Agado Agado Live Agado Rehab

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QKC	Interactive Rehabilitation Exercise Device, Prescription Use	Physical Medicine	Class 2	890.5360	2025-03-13

Official Correspondent

Vittaly Tavor

US Agent Details

David Volosov Email: sys@agadolive.com Phone: (410) 9608731

Related Public Records

Same Entity

Agado Live Ltd.

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 3038185754. Last updated year: 2026. Please use registration number 3038185754 when referencing this establishment in official correspondence.