MENICON CO. LTD. Global Logistics Center

FDA Device Registration & Listing · Yachiyo Chiba, JP · Registration 3033524682

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
3033524682
FEI Number
3033524682
Entity Name
MENICON CO. LTD. Global Logistics Center
City/State/Country
Yachiyo Chiba, JP
Establishment Address
1353-4, Kamikouya, Yachiyo Chiba 2760022, JP
Establishment Type(s)
Repack or Relabel 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

Menicon Z Large Diameter Menicon Z Irregular Cornea

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2011-08-30
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2008-10-31

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
3009104180 Menicon Singapore Pte. Ltd. Singapore South West, SG

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K963512 Benz Research and Development Corp. BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL 1997-07-31

Similar Registrations

Registration Number Establishment Name Location
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3005994941 SOLOTICA INDUSTRIA E COMERCIO LTDA Sao Paulo, BR
3010607087 Menicon Nect Co., Ltd., Gujo Plant Gujo Gifu, JP
1835957 ART OPTICAL CONTACT LENS, INC. Walker, MI, US
3025308027 BIOLENS LAB Mohammedia Mohammadia, MA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033524682. Last updated year: 2026. Please use registration number 3033524682 when referencing this establishment in official correspondence.
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