Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040334342

FEI Number

3040334342

Entity Name

PM (PARTNER MANUFACTURING) LTD

City/State/Country

Bar-lev Industrial Park Northern, IL

Establishment Address

10 Harotem St., Bar-lev Industrial Park Northern 2015600, IL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PM (Partner Manufacturing) LTD (Owner Number: 10093817)

Owner / Operator Contact Address

10 Harotem St., Bar-lev Industrial Park, IL-Z 2015600, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Prolive Rx Relivion

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JXK	Cranial Electrotherapy Stimulator To Treat Depression	Neurology	Class 3	882.5800	2026-03-17
PCC	Stimulator, Nerve, Electrical, Transcutaneous, For Migraine	Neurology	Class 2	882.5891	2025-07-15

Official Correspondent

Didi Shalom

US Agent Details

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

Related Public Records

Same Entity

PM (Partner Manufacturing) LTD

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0019-05	Health Directions, Inc	3	HealthPax (HP-1). Cranial Electrotherapy Stimulator

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040334342. Last updated year: 2026. Please use registration number 3040334342 when referencing this establishment in official correspondence.