Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012262775

FEI Number

3012262775

Entity Name

MAX MARA S.R.L.

City/State/Country

Reggio emilia, IT

Establishment Address

Via Guilia Maramotti, 4, Reggio emilia 42124, IT

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Max Mara S.R.L. (Owner Number: 10052213)

Owner / Operator Contact Address

Via Guilia Maramotti, 4, Reggio emilia, IT-RE 42124, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Max Mara, Elsav

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2024-12-11

Official Correspondent

Claudio BAGNI

US Agent Details

Brian Bono Business: Savino Del Bene USA Email: brian.bono@savinodelbene.com Phone: (646) 2079822

Related Public Records

Same Entity

Max Mara S.R.L.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012262775. Last updated year: 2026. Please use registration number 3012262775 when referencing this establishment in official correspondence.