Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008851924

FEI Number

3008851924

Entity Name

PRONAT INDUSTRIES LTD.

City/State/Country

Emek Hefer Ind. Park Haifa, IL

Establishment Address

18 Tzavei Hanachal St, Emek Hefer Ind. Park Haifa 38777, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Pronat Industries Ltd. (Owner Number: 10050256)

Owner / Operator Contact Address

18 Tzavei Hanachal St, Emek Hefer Ind. Park, IL-NOTA 38777, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Genio® Customer Electrode Trace Non-sterile Cover Bandage

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MNQ	Stimulator, Hypoglossal Nerve, Implanted, Apnea	Unknown	Class 3	N/A	2025-09-03
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2020-07-02
HMW	Drape, Microscope, Ophthalmic	General, Plastic Surgery	Class 2	878.4370	2019-07-24
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2015-10-26

Official Correspondent

George Hattub

US Agent Details

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

Related Public Records

Same Entity

Pronat Industries 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
K934333	3M Medical Products Group	3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE	1994-07-07
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0040-2025	Inspire Medical Systems Inc.	3	Inspire Model 4340 Respiratory Sensing Lead, component of the Inspire Upper Airway Stimulation (UAS) system.
Z-0041-2025	Inspire Medical Systems Inc.	3	Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway Stimulation (UAS) system.

Similar Registrations

Registration Number	Establishment Name	Location
3030499299	Inspire Medical Systems Inc	Golden Valley, MN, US
3017191859	NYXOAH SA	Mont-Saint-Guibert Brabant Wallon, BE
3030384719	Nyxoah SA Milmort	Herstal Liege, BE
3030384402	NYXOAH INC	Summit, NJ, US
1047843	ISOMEDIX OPERATIONS INC.	SPARTANBURG, SC, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008851924. Last updated year: 2026. Please use registration number 3008851924 when referencing this establishment in official correspondence.