Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015282628

FEI Number

3015282628

Entity Name

FOCUS PROVEEDORA SA DE CV

City/State/Country

San Pedro Garza Garcia Nuevo Leon, MX

Establishment Address

Ave. Ricardo Margain Zozaya #335 4th floor, Col. Valle del Campestre, San Pedro Garza Garcia Nuevo Leon 66265, MX

Establishment Type(s)

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

Owner / Operator

Focus Proveedora SA de CV (Owner Number: 10059822)

Owner / Operator Contact Address

Ave. Ricardo Margain Zozaya #335 4th floor, Col. Valle del Campestre, San Pedro Garza Garcia, MX-NLE 66265, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K113703

PMA Number

N/A

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	2019-02-28
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-03-13
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-03-13
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2019-03-06
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2022-02-18
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2022-02-18
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-11-21
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2019-11-21
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2022-06-08
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2022-06-08

Official Correspondent

Thelma Cantu

US Agent Details

Alvaro Idrobo Business: AlvaroIdrobo Email: alvari80@gmail.com Phone: (954) 8267072

Related Public Records

Same Entity

Focus Proveedora SA de CV

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 3015282628. Last updated year: 2026. Please use registration number 3015282628 when referencing this establishment in official correspondence.