BNL EUROLENS SA

FDA Device Registration & Listing · MONTANGES Ain, FR · Registration 3000189209

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
3000189209
FEI Number
3000189209
Entity Name
BNL EUROLENS SA
City/State/Country
MONTANGES Ain, FR
Establishment Address
Route de Montanges, MONTANGES Ain 01200, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BNL EUROLENS SA (Owner Number: 10028479)
Owner / Operator Contact Address
Route de Montanges, MONTANGES, FR-01 01200, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PC SOL-utions BNL EUROLENS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2018-02-06
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2009-02-04

Official Correspondent

Frederic DELICOURT

US Agent Details

M Shannon McMurrey Business: EssilorLuxottica Email: smcmurrey@essilorusa.com Phone: (972) 8005206

Related Public Records

Same Entity

BNL EUROLENS SA
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
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
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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1000428458 GKB OPHTHALMICS LIMITED - UNIT II North Goa Goa, IN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3000189209. Last updated year: 2026. Please use registration number 3000189209 when referencing this establishment in official correspondence.
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