LUNETTERIE GENERALE INC

FDA Device Registration & Listing · Repentigny Quebec, CA · Registration 3032246460

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
3032246460
FEI Number
3032246460
Entity Name
LUNETTERIE GENERALE INC
City/State/Country
Repentigny Quebec, CA
Establishment Address
436 Rue St Paul, Repentigny Quebec J5Z 4H9, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Lunetterie Generale Inc (Owner Number: 10092781)
Owner / Operator Contact Address
436 Rue St Paul, Repentigny, CA-QC J5Z 4H9, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lunetterie frames Lunetterie frames

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2025-02-18
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2025-02-18

Official Correspondent

Julien Couture

US Agent Details

Joseph Azary Business: Aztech Regulatory and Quality LLC Email: aztechregulatory@gmail.com Phone: (203) 2426670

Related Public Records

Same Entity

Lunetterie Generale Inc
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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032246460. Last updated year: 2026. Please use registration number 3032246460 when referencing this establishment in official correspondence.
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