ROGER EYE DESIGN

FDA Device Registration & Listing · Etten-Leur Noord-Brabant, NL · Registration 3009554831

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
3009554831
FEI Number
3009554831
Entity Name
ROGER EYE DESIGN
City/State/Country
Etten-Leur Noord-Brabant, NL
Establishment Address
Toernooiveld 87, Etten-Leur Noord-Brabant 874873 DJ, NL
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Roger Eye Design (Owner Number: 10061338)
Owner / Operator Contact Address
4873 DJ Etten-Leur, Toernooiveld 87, NL-NOTA 87, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Roger Eye Design

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2019-10-09

Official Correspondent

Roger Hoppenbrouwers

US Agent Details

Diana Mansour Email: billing@zoweewow.com Phone: (425) 8301651

Related Public Records

Same Entity

Roger Eye Design
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009554831. Last updated year: 2026. Please use registration number 3009554831 when referencing this establishment in official correspondence.
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