CREAPRODUCT SRL

FDA Device Registration & Listing · Como, IT · Registration 3031462230

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
3031462230
FEI Number
3031462230
Entity Name
CREAPRODUCT SRL
City/State/Country
Como, IT
Establishment Address
Via Antonio Magni 54, Como I-22100, IT
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Creaproduct Srl (Owner Number: 10093871)
Owner / Operator Contact Address
Via Antonio Magni 54, Como, IT-CO I-22100, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Exceed, 6-MNP 1.5 Exceed US, Bio Touch Precision, 6-MNP 1.5 Bio Touch Precision, Footswitch Exceed, 6-MNP 1.5 Exceed US, Bio Touch Precision, 6-MNP 1.5 Bio Touch Precision, Footswitch

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 2025-07-25
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2025-07-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Creaproduct 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 3031462230. Last updated year: 2026. Please use registration number 3031462230 when referencing this establishment in official correspondence.
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