CURATRONIC, LTD.

FDA Device Registration & Listing · JERUSALEM Central, IL · Registration 3004938911

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004938911
FEI Number
3004938911
Entity Name
CURATRONIC, LTD.
City/State/Country
JERUSALEM Central, IL
Establishment Address
101 HEBRON ROAD, JERUSALEM Central 9348001, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CURATRONIC, LTD. (Owner Number: 9069104)
Owner / Operator Contact Address
101 HEBRON ROAD, --, JERUSALEM, IL-NOTA 9348001, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K042650
PMA Number
N/A

All Registered Proprietary Names

Biomove 5000 Parmods Biomove 3000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2008-07-30
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2012-08-27
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2007-12-12

Official Correspondent

No official correspondent registered.

US Agent Details

Naphtali Deutsch Business: A. STEIN - REGULATORY AFFAIRS CONSULTING LTD. Email: ahava@asteinrac.com Phone: (888) 4433867

Related Public Records

Same Entity

CURATRONIC, 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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004938911. Last updated year: 2026. Please use registration number 3004938911 when referencing this establishment in official correspondence.
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