Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009304068

FEI Number

3009304068

Entity Name

ENDOSPAN LTD

City/State/Country

Herzliya Central, IL

Establishment Address

4 Maskit St, Herzliya Central 4673304, IL

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Endospan (Owner Number: 10095741)

Owner / Operator Contact Address

4 Maskit St, Herzeliya Business Park, Herzliya, IL-M 4673304, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P250033

All Registered Proprietary Names

NEXUS Aortic Arch Stent Graft System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SDZ	Endovascular System For Treatment Of Ascending Aorta And Aortic Arch Lesions	Unknown	Class 3	N/A	2026-04-22

Official Correspondent

No official correspondent registered.

US Agent Details

Jill Munsinger Business: Gateway Medical Consulting Services Email: jmunsinger@gatewayMCS.com Phone: (651) 2700572

Related Public Records

Same Entity

Endospan

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009304068. Last updated year: 2026. Please use registration number 3009304068 when referencing this establishment in official correspondence.