Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025414414

FEI Number

3025414414

Entity Name

SHENZHEN DASHICHENG OPTICAL TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

101, 201 and 301, Unit 3, Building 1, Wanjiening Industrial Park, No. 1450, Guanguang Road, Jutang Community, Fucheng Sub-district, Longhua District, Shenzhen Guangdong 518110, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Dashicheng Optical Technology Co., Ltd. (Owner Number: 10086448)

Owner / Operator Contact Address

101, 201 and 301, Unit 3, Building 1, Wanjiening Industrial Park, No. 1450, Guanguang Road, Jutang Community, Fucheng Sub-district, Longhua District, Shenzhen, CN-GD 518110, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K220143

PMA Number

N/A

All Registered Proprietary Names

miiemo, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, model: BARBIE MOODY, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, model: BARBIE Unicoeye, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, model: BARBIE color contact lens, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, BARBIE Huneyes, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, Model: BARBIE DSC, BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens, Model: BARBIE

Registered Product Listings

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

Official Correspondent

Jiayi Li

US Agent Details

Anna SUN Business: SUN LUNA STAR LLC Email: usa@medpath.pro Phone: (626) 2005096

Related Public Records

Same Entity

Shenzhen Dashicheng Optical Technology 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
3008034930	VASSEN CO., LTD.	Pyeongtaek-si Gyeonggi, KR
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
3026035637	Innova Vision Inc.	Hsinchu City, Hsinchu (City), TW

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025414414. Last updated year: 2026. Please use registration number 3025414414 when referencing this establishment in official correspondence.