DE RIGO VISION S.P.A.

FDA Device Registration & Listing · LONGARONE (BL) Belluno, IT · Registration 3005246919

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
3005246919
FEI Number
3005246919
Entity Name
DE RIGO VISION S.P.A.
City/State/Country
LONGARONE (BL) Belluno, IT
Establishment Address
12, ZONA INDUSTRIALE VILLANOVA, LONGARONE (BL) Belluno 32013, IT
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
DE RIGO VISION S.P.A. (Owner Number: 9008492)
Owner / Operator Contact Address
12, ZONA INDUSTRIALE VILLANOVA, --, LONGARONE (BL), IT-BL 32013, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

De Rigo Vision Spa Zadig&Voltaire Porsche Design Chopard Escada Sting Yalea Mulberry Lozza Twinset Rodenstock Furla Tous Police Blumarine Philipp Plein Nina Ricci Roberto Cavalli Just Cavalli Plein Sport AG Fila De Rigo Vision Spa De Rigo Vision Spa

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2023-03-28
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 1993-12-01
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2023-03-27

Official Correspondent

MICHELE ARACRI

US Agent Details

Lisa Wright Business: THE VISION COUNCIL Email: fda@thevisioncouncil.org Phone: (703) 5484560

Related Public Records

Same Entity

DE RIGO VISION S.P.A.
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 3005246919. Last updated year: 2026. Please use registration number 3005246919 when referencing this establishment in official correspondence.
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