MESA ITALIA S.R.L.

FDA Device Registration & Listing · TRAVAGLIATO Brescia, IT · Registration 3010388903

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
3010388903
FEI Number
3010388903
Entity Name
MESA ITALIA S.R.L.
City/State/Country
TRAVAGLIATO Brescia, IT
Establishment Address
VIA DELL ARTIGIANATO 35-37-39, TRAVAGLIATO Brescia 25039, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Mesa Italia S.r.l. (Owner Number: 10044677)
Owner / Operator Contact Address
VIA DELL'ARTIGIANATO 35-37, TRAVAGLIATO, IT-BS 25039, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MAGNUM ALBUM MAGNUM MICANS MAGNUM SPLENDIDUM MAGNUM SIMPLEX MAGNUM SALDATURA Co MAGNUM SALDATURA A MAGNUM SALDATURA W MAGNUM NITENS MAGNUM ADAMANTA 2 MAGNUM VIP-A MAGNUM CLARUM MAGNUM H60 MAGNUM CERAMIC S MAGNUM H50 MAGNUM LUCENS MAGNUM SALDATURA Ni-Cr MAGNUM SUAVE MAGNUM CERALBUM MAGNUM VIP MAGNUM SALDATURA B MAGNUM HBA MAGNUM H100 MAGNUM H65 MAGNUM CERAMIC Co MAGNUM FULGENS MAGNUM H75 MAGNUM SOLARE MAGNUM SATURNO MAGNUM HYPERONE MAGNUM Ni-Cr-Fe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJH Alloy, Metal, Base Dental Class 2 872.3710 2013-07-12

Official Correspondent

GIACOMO SALA

US Agent Details

Jean Bigoney Business: Nu Device Consulting LLC Email: info@nu-device.com Phone: (919) 2081953

Related Public Records

Same Entity

Mesa Italia S.r.l.
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
K810521 C.Vaupel Dental, Inc. CO-SPAN 13.5 CASTING ALLOY 1981-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010388903. Last updated year: 2026. Please use registration number 3010388903 when referencing this establishment in official correspondence.
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