MATTIOLI ENGINEERING ITALIA SRL

FDA Device Registration & Listing · Calenzano Firenze, IT · Registration 9680612

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
9680612
FEI Number
1000390170
Entity Name
MATTIOLI ENGINEERING ITALIA SRL
City/State/Country
Calenzano Firenze, IT
Establishment Address
Via San Morese 80, Calenzano Firenze 50041, IT
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MATTIOLI ENGINEERING LTD. (Owner Number: 9035865)
Owner / Operator Contact Address
37 - 38 Long Acre, --, LONDON, GB-LND WC2E 9JT, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K042590
PMA Number
N/A

All Registered Proprietary Names

Device, iontophoresis, other uses Transderm Ionto Transderm Ionto DEP DEP SYSTEM PRO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2007-11-28

Official Correspondent

No official correspondent registered.

US Agent Details

Rich WYNKOOP Business: Vision28 Email: rich@vision28.com Phone: (541) 6049654

Related Public Records

Same Entity

MATTIOLI ENGINEERING LTD.
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
K842483 Santa Barbara Medco, Inc. SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC 1984-08-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680612. Last updated year: 2026. Please use registration number 9680612 when referencing this establishment in official correspondence.
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