Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010413909

FEI Number

3010413909

Entity Name

Menicon Nect Co., Ltd.

City/State/Country

Nagoya Aichi, JP

Establishment Address

390, Ichibagi-cho, Nishi-ku, Nagoya Aichi 452-0805, JP

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

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

Expiration Date (Year)

2026

510(k) Number

K131875

PMA Number

N/A

All Registered Proprietary Names

Menicon Nect Contact Lens Case

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRX	Case, Contact Lens	Ophthalmic	Class 2	886.5928	2013-08-27

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
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
3014769028	Menicon Co., Ltd. Techno-station	Kakamigahara Gifu, JP

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010413909. Last updated year: 2026. Please use registration number 3010413909 when referencing this establishment in official correspondence.