Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015088397

FEI Number

3015088397

Entity Name

NEUROLIEF Ltd.

City/State/Country

Netanya Central, IL

Establishment Address

12 Giborei Israel, Netanya Central 4250412, IL

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Neurolief (Owner Number: 10081665)

Owner / Operator Contact Address

12 Giborei Israel, Netanya, IL-M 4250412, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P250010

All Registered Proprietary Names

Relivion ProlivRx System ProlivRx external Combined Occipital and Trigeminal Afferent Stimulation (eCOT-AS)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PCC	Stimulator, Nerve, Electrical, Transcutaneous, For Migraine	Neurology	Class 2	882.5891	2021-05-18
JXK	Cranial Electrotherapy Stimulator To Treat Depression	Neurology	Class 3	882.5800	2026-01-18

Official Correspondent

Dganit Litinsky

US Agent Details

Lewis Steve Beller Business: Neurolief Inc. Email: Steve.beller@neurolief.com Phone: (210) 8436778

Related Public Records

Same Entity

Neurolief

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3019551144	NEUROLIEF Inc.	Coral Springs, FL, US

Related Recall Records

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

Similar Registrations

Registration Number	Establishment Name	Location
3016856381	Hinge Health Inc.	San Francisco, CA, US
3014649088	WAT MEDICAL TECHNOLOGY INC.	Ningbo Zhejiang, CN
3010188009	CEFALY TECHNOLOGY	Liege, BE
3005170249	Shenzhen Dongdixin Technology Co., Ltd.	SHENZHEN Guangdong, CN
3019551144	NEUROLIEF Inc.	Coral Springs, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015088397. Last updated year: 2026. Please use registration number 3015088397 when referencing this establishment in official correspondence.