Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018901422

FEI Number

3018901422

Entity Name

LINKVERSE S.R.L.

City/State/Country

Roma, IT

Establishment Address

Via Ostiense 131L, Roma 00154, IT

Establishment Type(s)

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

Owner / Operator

Linkverse s.r.l. (Owner Number: 10081308)

Owner / Operator Contact Address

Via Ostiense 131L, Roma, IT-RM 00154, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241887

PMA Number

N/A

All Registered Proprietary Names

ColonPRO 4 Footswitch GI Genius Module 200 GI Genius Module 100 USB K-switch ColonPRO 4 (CPRO401S-US) ColonPRO 4 (CPRO40S-US) GI Genius Module 300 GI Genius Module 100 GI Genius Module 200 ColonPRO 4 (CPRO40.US) ColonPRO US (CPRO402S-US)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QNP	Gastrointesinal Lesion Software Detection System	Gastroenterology, Urology	Class 2	876.1520	2024-02-16
QNP	Gastrointesinal Lesion Software Detection System	Gastroenterology, Urology	Class 2	876.1520	2024-09-12

Official Correspondent

No official correspondent registered.

US Agent Details

Steve Kradjian Business: Conventus Biomedical Solutions Email: skradjian@conventusbiomed.com Phone: (858) 4012111

Related Public Records

Same Entity

Linkverse s.r.l.

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 3018901422. Last updated year: 2026. Please use registration number 3018901422 when referencing this establishment in official correspondence.