FEOPS NV

FDA Device Registration & Listing · Gent Oost-Vlaanderen, BE · Registration 3020703662

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
3020703662
FEI Number
3020703662
Entity Name
FEOPS NV
City/State/Country
Gent Oost-Vlaanderen, BE
Establishment Address
Technologiepark-Zwijnaarde 122, Gent Oost-Vlaanderen 9052, BE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FEops NV (Owner Number: 10082838)
Owner / Operator Contact Address
Technologiepark-Zwijnaarde 122, Gent, BE-VOV 9052, BE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223855
PMA Number
N/A

All Registered Proprietary Names

FEops HEARTguide FEops HEARTguide Simulation Application v1.4.2 FEops HEARTguide Simulation Application FEops HEARTguide Simulation Application v4.1 FEops HEARTguide FEops HEARTguide ALPACA FEops HEARTguide FEops HEARTguide ALPACA 3.3

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QQI Interventional Cardiovascular Implant Simulation Software Device Cardiovascular Class 2 870.1405 2021-10-07
QQI Interventional Cardiovascular Implant Simulation Software Device Cardiovascular Class 2 870.1405 2022-03-14
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2023-06-14

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

FEops NV
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
K242270 Orthofix Srl OrthoNext Platform System 2024-12-19
K261713 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.6.0) 2026-06-18
K243647 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.5) 2025-06-30

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3042852277 REMEDY LOGIC New York, NY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020703662. Last updated year: 2026. Please use registration number 3020703662 when referencing this establishment in official correspondence.
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