Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013521567

FEI Number

3013521567

Entity Name

DOSENTRX LTD.

City/State/Country

Modiin-Maccabim-Reut Central, IL

Establishment Address

1 HaMaayan St., Modiin-Maccabim-Reut Central 7177874, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dosentrx Ltd. (Owner Number: 10054587)

Owner / Operator Contact Address

1 HaMaayan St., Modiin-Maccabim-Reut, IL-M 7177874, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ReX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2017-04-05

Official Correspondent

Mishelle Voronin

US Agent Details

MARK SUMMERS Email: msummers@dosentrx.com Phone: (612) 8170959

Related Public Records

Same Entity

Dosentrx 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
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013521567. Last updated year: 2026. Please use registration number 3013521567 when referencing this establishment in official correspondence.