Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000576299

FEI Number

1000576299

Entity Name

LEBANESE INTERNATIONAL TECHNOLOGIES

City/State/Country

MAZRAET YACHOUH Liban-Nord, LB

Establishment Address

BELOW MERALCO CENTER, MAZRAET YACHOUH Liban-Nord --, LB

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

LEBANESE INTERNATIONAL TECHNOLOGIES (Owner Number: 9071915)

Owner / Operator Contact Address

BELOW MERALCO CENTER, --, MAZRAET YACHOUH, LB-NOTA --, LB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cetro America

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGM	System, Monitoring, Perinatal	Obstetrics/Gynecology	Class 2	884.2740	2007-08-27

Official Correspondent

No official correspondent registered.

US Agent Details

Maya Cianciolo Business: CETRO AMERICA, INC. Email: admin@cetroamerica.com Phone: (203) 4400064

Related Public Records

Same Entity

LEBANESE INTERNATIONAL TECHNOLOGIES

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
K771196	Hewlett-Packard Co.	MARKER GENERATOR MODULES - 21597A	1977-08-03
K813458	Cranbury Medical Labs, Inc.	FETASCAN 1000, 1000A OBSTETRICAL DATA	1982-01-28
K100420	Philips Medizin Systeme Boeblingen GmbH	PHILIPS OBTRACEVUE MODEL SW REV. G.00	2010-07-26
K173941	Philips Medizin Systeme Boeblingen GmbH	IntelliSpace Perinatal Rev.K.00	2018-09-10
K062137	Philips Medizin Systeme Boeblingen GmbH	MODIFICATION TO PHILIPS AVALON FETAL MONITORS FM20 AND FM30	2006-08-24

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0035-06	N/A	2	FETALGARD Lite Fetal Monitors, Model AP1S (Single Fetus Monitoring)
Z-0036-06	N/A	2	FETALGARD Lite Fetal Monitors, Model HCS (Home Care Single Fetus Monitoring)

Similar Registrations

Registration Number	Establishment Name	Location
3008403701	TENACORE LLC	Costa Mesa, CA, US
3004167720	CETRO AMERICA	Meriden, CT, US
3009499478	EDAN Diagnostics, Inc.	San Diego, CA, US
1424263	Isomedix Operations, Inc.	Libertyville, IL, US
3007734888	WIPRO GE HEALTHCARE PRIVATE Ltd.	BANGALORE Karnataka, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000576299. Last updated year: 2026. Please use registration number 1000576299 when referencing this establishment in official correspondence.