JULBO

FDA Device Registration & Listing · LONGCHAUMOIS Jura, FR · Registration 3004048512

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
3004048512
FEI Number
3004048512
Entity Name
JULBO
City/State/Country
LONGCHAUMOIS Jura, FR
Establishment Address
ZABP2, LONGCHAUMOIS Jura 39400, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
JULBO (Owner Number: 9037885)
Owner / Operator Contact Address
296 Avenue D, Suite 10, Williston, VT 05495, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

JULBO Rextrem

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2003-05-08
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2014-05-27

Official Correspondent

Marc Bryce

US Agent Details

Marc Bryce Business: JULBO, INC Email: accounting@JULBOUSA.COM Phone: (802) 6510833

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3013462840 SC FILTROPTIC SRL MINTIA Hunedoara, RO

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004048512. Last updated year: 2026. Please use registration number 3004048512 when referencing this establishment in official correspondence.
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