Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030126381

FEI Number

3030126381

Entity Name

NURAMI MEDICAL LTD

City/State/Country

Haifa, IL

Establishment Address

36, Ha-Namal, Haifa 3303203, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Nurami Medical Ltd (Owner Number: 10089552)

Owner / Operator Contact Address

Hanamal 36, Haifa, IL-HA 32000, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223445

PMA Number

N/A

All Registered Proprietary Names

ArtiFascia 3X4 ArtiFascia 5X5 ArtiFascia 7X7

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GXQ	Dura Substitute	Neurology	Class 2	882.5910	2023-12-17

Official Correspondent

Nora Nseir

US Agent Details

Jeanine Faust Business: Nurami Medical, Inc. Email: jfaust@ubsmed.com Phone: (610) 3171670

Related Public Records

Same Entity

Nurami Medical Ltd

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 3030126381. Last updated year: 2026. Please use registration number 3030126381 when referencing this establishment in official correspondence.