Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030421258

FEI Number

3030421258

Entity Name

ENLACES CORPORATIVOS 55 DEL NORTE S.A. DE C.V.

City/State/Country

MEXICO Ciudad de Mexico, MX

Establishment Address

PASEO DE SAN FRANCISCO 105 COL JARDINES DE ATIZAPAN, MUNICIPIO ATIZAPAN DE ZARAGOZA, MEXICO Ciudad de Mexico 52978, MX

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

ENLACES CORPORATIVOS 55 DEL NORTE S.A. DE C.V. (Owner Number: 10089687)

Owner / Operator Contact Address

PASEO DE SAN FRANCISCO 105 COL JARDINES DE ATIZAPAN, MUNICIPIO ATIZAPAN DE ZARAGOZA, MEXICO, MX-CMX 52978, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P180035

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-11-21
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-01-08
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2024-01-08
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2024-01-08
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-11-21
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2024-11-21
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2024-05-15
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2024-01-08
NAD	Dressing, Wound, Occlusive	General, Plastic Surgery	Class 1	878.4020	2025-03-13
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2023-12-28
QIT	Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia	Unknown	Class 3	N/A	2026-05-28

Official Correspondent

FRANCISCO PUENTE QUINONES

US Agent Details

Andrea Diaz Email: nicole@gcbusa.com Phone: (786) 2228896

Related Public Records

Same Entity

ENLACES CORPORATIVOS 55 DEL NORTE S.A. DE C.V.

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
K133079	Alden Optical Labs., Inc.	IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC)	2013-12-17
K941998	Ocu-Ease Optical Products, Inc.	OCU-FLEX-38 (POLYMACON)	1994-10-13
K992500	Cantor & Silver , Ltd.	CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS	1999-08-18
K984098	Adventures IN Color Technology, Ltd.	ADVENTURE TINTS, COLOR ENHANCED TINTED SOFT CONTACT LENS	1999-05-10
K003161	Les Laboratoires Blanchard	ESSTECH MULTI TORIC ASPHERIC (MULTIFOCAL) (HIOXIFILCON B) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR (CLEAR AND TINT	2000-12-15

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0018-07	Ciba Vision Corporation	2	CSI Daily Wear, soft (hydrophilic) contact lenses
Z-0019-07	Ciba Vision Corporation	2	CSI Flexible Wear, soft (hydrophilic) contact lenses
Z-0020-07	Ciba Vision Corporation	2	CSI Toric, soft (hydrophilic) contact lenses
Z-0044-2012	CooperVision Inc.	2	AVAIRA Toric (enfilcon A) TORIC soft (Hydrophilic) Contact Lenses, 6 SOFT CONTACT LENSES FOR ASTIGMATISM, CooperVision, Scottsville, NY 14546 USA; Juana Diaz, PR 00795 USA; Hamble SO31, 4RF, UK; Device Listing # D033736. Product Usage: Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from -20.00- to +20.00 diopters and astigmatic corrections from -0.25 to -10.00 diopters. The AVAIRA Soft Contact Lens is indicated for single - use disposable wear and daily wear. When prescribed for frequent replacement, the lens may be disinfected using a chemical or hydrogen peroxide disinfecting system.
Z-0326-2026	Alcon Research LLC	2	Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030421258. Last updated year: 2026. Please use registration number 3030421258 when referencing this establishment in official correspondence.