Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013170070

FEI Number

3013170070

Entity Name

UNICON OPTICAL CO., LTD.

City/State/Country

Hsinchu County, TW

Establishment Address

No.16, Gongye E. 9th Rd., Hsinchu Science Park, Baoshan Township, Hsinchu County 30075, TW

Establishment Type(s)

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

Owner / Operator

Unicon Optical Co., Ltd. (Owner Number: 10052876)

Owner / Operator Contact Address

No.16, Gongye E. 9th Rd., Hsinchu Science Park, Baoshan Township, Hsinchu County, TW-HSQ 30075, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K213216

PMA Number

N/A

All Registered Proprietary Names

Unicon (Etafilcon A) Soft (hydrophilic) Contact Lens with UV Blocker for Daily Wear UNICON Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact Lens To be notified Ivision Qualis Alice Silicone 1-Day Alice Silicone Bi-weekly Soft Contact Lens

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2016-10-13
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2016-10-13
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2019-11-13
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2019-11-13
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2022-04-11
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2022-04-11

Official Correspondent

Will Wang

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Unicon Optical Co., 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.

Similar Registrations

Registration Number	Establishment Name	Location
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3043022738	METI OPTICAL INC	Dover, DE, US
3012760082	Maxvue Vision Sdn. Bhd.	Seremban Negeri Sembilan, MY
3010640396	KELABIT S.R.O.	Ostrava Moravskoslezsky Kraj, CZ

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013170070. Last updated year: 2026. Please use registration number 3013170070 when referencing this establishment in official correspondence.