I.O.V.E.S. SPA

FDA Device Registration & Listing · LOZZO DI CADORE Belluno, IT · Registration 3002900744

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
3002900744
FEI Number
3002900744
Entity Name
I.O.V.E.S. SPA
City/State/Country
LOZZO DI CADORE Belluno, IT
Establishment Address
VIA DELL INDUSTRIA 9, LOZZO DI CADORE Belluno 32040, IT
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
I.O.V.E.S. SPA (Owner Number: 10044408)
Owner / Operator Contact Address
VIA DELL INDUSTRIA 9, LOZZO DI CADORE, IT-BL 32040, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AMARCORD WEST DIVA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2013-06-06

Official Correspondent

RODOLFO COSTAN

US Agent Details

MATTIA COSTAN Business: IOVES USA Email: info@ioves-usa.com Phone: (213) 5983788

Related Public Records

Same Entity

I.O.V.E.S. SPA
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 3002900744. Last updated year: 2026. Please use registration number 3002900744 when referencing this establishment in official correspondence.
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