Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010361494

FEI Number

3010361494

Entity Name

Tavger Ltd.

City/State/Country

Katzrin Ha Zafon Haifa, IL

Establishment Address

4 Alonim St., Katzrin Ha Zafon Haifa 12-90000, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tavger Ltd (Owner Number: 10044450)

Owner / Operator Contact Address

4 Alonim St, POB 83, Katzrin, Ha Zafon, IL-NOTA 12900, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Affinity MesoStrip Affinity GJS Affinity Mini Affinity Derm BioRef-DC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQH	Lavage, Jet	General Hospital	Class 2	880.5475	2013-06-13
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2019-11-15

Official Correspondent

Michael Tavger

US Agent Details

Yelena Mashkevich Email: ymashkevich@yahoo.com Phone: (215) 4072239

Related Public Records

Same Entity

Tavger 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
K213616	Becton, Dickinson and Company	BD Surgiphor Antimicrobial Irrigation System	2022-03-23
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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010361494. Last updated year: 2026. Please use registration number 3010361494 when referencing this establishment in official correspondence.