Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011521050

FEI Number

3011521050

Entity Name

SHOTLEY LIMITED

City/State/Country

Kowloon, HK

Establishment Address

Unit 706, 7/F, South Seas Centre Tower 2, No.75 Mody Road, Tsim Sha Tsui, Kowloon None, HK

Establishment Type(s)

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

Owner / Operator

SHOTLEY LIMITED (Owner Number: 10060972)

Owner / Operator Contact Address

SHOTLEY LIMITED, Room 801-803, Park Sun Building., No.97-107 Wo Yi Hop Road,, Kwai Chung, N.T., HK-NOTA None, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K143632

PMA Number

N/A

All Registered Proprietary Names

Acuvue Oasys Max 1 Day Multifocal 1 Day Acuvue Moist 1 Day Acuvue Moist for Astigmatism 1 Day Acuvue Moist Multifocal Acuvue Oasys 1 Day for Astigmatism Acuvue Oasys Acuvue Oasys for Astigmatism ACUVUE OASYS 1-Day with HydraLuxe Proclear 1 Day Biotrue ONEday Acuvue Oasys Multifocal Biofinity Biofinity Toric Biofinity Multifocal Biotrue ONEday for Astigmatism

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	2019-07-26
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-07-23
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2023-12-10
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2023-12-10
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
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2026-02-20
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2026-02-20
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-07-26
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2019-07-26
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2025-04-29
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2025-04-29
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-07-26
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2026-02-20
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2026-02-20

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

SHOTLEY LIMITED

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 3011521050. Last updated year: 2026. Please use registration number 3011521050 when referencing this establishment in official correspondence.