Menicon Singapore Pte. Ltd.

FDA Device Registration & Listing · Singapore South West, SG · Registration 3009104180

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009104180
FEI Number
3009104180
Entity Name
Menicon Singapore Pte. Ltd.
City/State/Country
Singapore South West, SG
Establishment Address
8 International Business Park, Singapore South West 609925, SG
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MENICON CO. LTD. (Owner Number: 9001029)
Owner / Operator Contact Address
21-19 AOI, 3-CHOME, NAKA-KU, --, NAGOYA, JP-23 460-0006, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Miru 1day Menicon Flat Pack Toric Miru 1day Menicon Flat Pack

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 2011-05-08

Official Correspondent

Zhu Jiang

US Agent Details

Alberty Recio Business: MENICON AMERICA, INC. Email: alberty_recio@menicon.com Phone: (781) 6092042

Related Public Records

Same Entity

MENICON CO. LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011861185 Menicon Singapore Pte. Ltd. (Site 2) SINGAPORE South West, SG
3010413909 Menicon Nect Co., Ltd. Nagoya Aichi, JP
3002807570 Menicon Co., Ltd., Seki Plant Seki Gifu, JP
3014768085 Menicon Co., Ltd., Kakamigahara Plant Kakamigahara Gifu, JP
3014769028 Menicon Co., Ltd. Techno-station Kakamigahara Gifu, JP

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 3009104180. Last updated year: 2026. Please use registration number 3009104180 when referencing this establishment in official correspondence.
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