Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042225401

FEI Number

3042225401

Entity Name

CAMPOMATS

City/State/Country

Riccione Rimini, IT

Establishment Address

Via Monte Rosa 11, Riccione Rimini 47838, IT

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

CAMPOMATS (Owner Number: 10094413)

Owner / Operator Contact Address

Via Monte Rosa 11, Riccione, IT-RN 47838, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243472

PMA Number

N/A

All Registered Proprietary Names

1NEED Pro

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QAI	Powered Microneedle Device	General, Plastic Surgery	Class 2	878.4430	2025-11-27

Official Correspondent

Elisa Campomagnani

US Agent Details

Jay Mansour Business: Mansour Consulting LLC Email: jay@mansourconsulting.com Phone: (678) 9088108

Related Public Records

Same Entity

CAMPOMATS

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 3042225401. Last updated year: 2026. Please use registration number 3042225401 when referencing this establishment in official correspondence.