PULSENMORE LTD

FDA Device Registration & Listing · Omer Southern, IL · Registration 3020542149

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
3020542149
FEI Number
3020542149
Entity Name
PULSENMORE LTD
City/State/Country
Omer Southern, IL
Establishment Address
8 Omarim St., Omer Southern 8496500, IL
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Pulsenmore LTD (Owner Number: 10094113)
Owner / Operator Contact Address
8 Omarim st., Omer, IL-D 8496500, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Pulsenmore ES

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SGJ Ultrasound Imaging System For Acquiring Images At Home By Lay Users Radiology Class 2 892.1590 2025-11-15

Official Correspondent

ISRAEL CITRON

US Agent Details

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

Related Public Records

Same Entity

Pulsenmore LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020542149. Last updated year: 2026. Please use registration number 3020542149 when referencing this establishment in official correspondence.
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