EVO DI BRIDDA MASSIMO

FDA Device Registration & Listing · SEDICO Belluno, IT · Registration 3010862420

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
3010862420
FEI Number
3010862420
Entity Name
EVO DI BRIDDA MASSIMO
City/State/Country
SEDICO Belluno, IT
Establishment Address
VIA FELTRE 52/M, SEDICO Belluno 32036, IT
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device for Another Party (Contract Manufacturer),Remanufacture Medical Device,Foreign Private Label Distributor,Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device,Sterilize Medical Device for Another Party (Contract Sterilizer),Develop Specifications But Do Not Manufacture At This Facility,Reprocess Single-Use Device
Owner / Operator
EVO DI BRIDDA MASSIMO (Owner Number: 10046465)
Owner / Operator Contact Address
VIA FELTRE 52/M, SEDICO, IT-BL 32036, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EVO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2016-12-23
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2014-03-26

Official Correspondent

MASSIMO BRIDDA

US Agent Details

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

Related Public Records

Same Entity

EVO DI BRIDDA MASSIMO
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 3010862420. Last updated year: 2026. Please use registration number 3010862420 when referencing this establishment in official correspondence.
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