Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010890435

FEI Number

3010890435

Entity Name

ANGEL EYE CENTRE LTD.

City/State/Country

Wembley Brent, GB

Establishment Address

6 & 7 Tower Business Park, Carey Way, Wembley Brent HA90LQ, GB

Establishment Type(s)

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

Owner / Operator

ANGEL EYE CENTRE LTD. (Owner Number: 10046533)

Owner / Operator Contact Address

6 & 7 Tower Business Park, Carey Way, Wembley, GB-NOTA HA90LQ, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K113168

PMA Number

N/A

All Registered Proprietary Names

1 Day Acuvue Moist Multifocal FRESHLOOK DIMENSION Total30 Asphere Total30 Multifocal Total30 Total30 for Astigmatism Total30 Multifocal Toric Acuvue Vita for Astigmatism Acuvue Vita Dailies Total 1 For Astigmatism Dailies Total 1 Multifocal PureVision 2 for Astigmatism PUREVISION 2 PureVision 2 for Presbyopia Clariti 1 Day Toric Clariti 1 Day Clariti 1 Day Multifocal Biotrue ONEday Biotrue ONEday for Presbyopia Biotrue ONEday for Astigmatism Acuvue Advance Precision 1 Spherical Biofinity Energys Biofinity Toric Biofinity Biofinity Multifocal PROCLEAR MULTIFOCAL PROCLEAR TORIC PROCLEAR 1 DAY SofLens Daily Disposable SofLens 38 Acuvue Oasys For Presbyopia ACUVUE OASYS 1-Day with HydraLuxe Acuvue Oasys Multifocal Acuvue Oasys For Astigmatism Avaira Vitality Avaira Vitality Toric FRESHLOOK 1 DAY Acuvue Oasys Max 1-Day Multifocal Acuvue Oasys Max 1-Day Acuvue Oasys Transitions ACUVUE OASYS Acuvue Oasys 1 Day for Astigmatism FreshLook ColorBlends PROCLEAR Bausch & Lomb Ultra One Day Air Optix Colors MyDay Acuvue Oasys Max 1-Day Acuvue 2 1 Day Acuvue Moist 1 Day Acuvue Define ACUVUE OASYS MAX 1-Day MULTIFOCAL 1 Day Acuvue Moist For Astigmatism FREQUENCY 55 ASPHERIC Dailies Total 1

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	2023-12-07
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2014-04-03
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-08-01
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2024-08-01
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-07
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-07
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-06-25
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2024-06-25
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2014-04-03
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2020-03-05
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2020-03-05
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-07
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-07
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2014-04-03
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2014-04-03
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-07-23
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2024-07-23
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2014-04-03
LPM	Lenses, Soft Contact, Extended Wear	Ophthalmic	Class 3	886.5925	2014-04-03
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-04
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-04
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-07
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-07
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2014-04-03
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2025-05-05
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2025-05-05
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2022-03-07
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2022-03-07
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-06-10
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-09-06
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-09-06
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2026-03-17
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2026-03-17
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-07-23
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-04
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-04
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2022-03-01
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2014-04-03
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2024-04-25
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2024-04-25

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

ANGEL EYE CENTRE 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
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 3010890435. Last updated year: 2026. Please use registration number 3010890435 when referencing this establishment in official correspondence.