Neuron Guard SRL

FDA Device Registration & Listing · Vignola Modena, IT · Registration 3030387297

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
3030387297
FEI Number
3030387297
Entity Name
Neuron Guard SRL
City/State/Country
Vignola Modena, IT
Establishment Address
via per Sassuolo 3853, Vignola Modena 41058, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Neuron Guard SRL (Owner Number: 10089621)
Owner / Operator Contact Address
via Ludovico Castelvetro 19, Modena, IT-MO 41121, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CB240_Aurora CB240C

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2023-12-22

Official Correspondent

Enrico Giuliani

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Neuron Guard SRL
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 3030387297. Last updated year: 2026. Please use registration number 3030387297 when referencing this establishment in official correspondence.
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