Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008034930

FEI Number

3008034930

Entity Name

VASSEN CO., LTD.

City/State/Country

Pyeongtaek-si Gyeonggi, KR

Establishment Address

50, Seotan-ro, Jinwi-myeon, Pyeongtaek-si Gyeonggi 17706, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Vassen Co., Ltd. (Owner Number: 10047683)

Owner / Operator Contact Address

50, Seotan-ro, Jinwi-myeon, Pyeongtaek-si, KR-41 17706, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K141699

PMA Number

N/A

All Registered Proprietary Names

Kitty Kawaii Hya Contact Lens Oneday le reve I POP Natural I Soda Natural Paris Lenses I Soda Colors DAHAB SHILLS PROFESSIONAL freshlens Ora Eva Lens TinkerBell Vassen Color Celeb Elite Glow I POP colors Wonder Look PARIS LENSES Lady U Lense I Soda Clear Savory Owl GLENSE Karma Naturel Paris Luminous I Kocktail Circle I Loco For Party Eagle Eye MyLens Beauteous SHILLS FAIRY Circle Venus 3D Colors MYSTERY Kitty Kawaii Plus Kitty Kawaii Hya Contact Lens Monthly

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	2014-10-20
MVN	Lens, Contact, (Disposable)	Ophthalmic	Class 2	886.5925	2014-10-20

Official Correspondent

Chung Hwan Park

US Agent Details

Bret Andre Business: EyeReg Consulting, Inc. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

Vassen 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
3013785060	CAMDEN PASSAGE	Collingwood Ontario, CA
3008585940	GEO MEDICAL CO., LTD	Buk-gu Gwangju, KR
3005994941	SOLOTICA INDUSTRIA E COMERCIO LTDA	Sao Paulo, BR
3012590738	EYEYON MEDICAL	Nes Ziona Central, IL
3025414414	SHENZHEN DASHICHENG OPTICAL TECHNOLOGY CO., LTD.	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008034930. Last updated year: 2026. Please use registration number 3008034930 when referencing this establishment in official correspondence.