Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2183926

FEI Number

1000116130

Entity Name

Merge Healthcare Incorporated

City/State/Country

Hartland, WI, US

Establishment Address

900 Walnut Ridge Dr, Hartland, WI 53029, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Merge Healthcare (Owner Number: 10024020)

Owner / Operator Contact Address

900 Walnut Ridge Drive, Hartland, WI 53029, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K233326

PMA Number

N/A

All Registered Proprietary Names

Merge OrthoCase Merge Hemo Merge Eye Care PACS Merge Cardio iConnect Access Merge OrthoTemplates Merge Cardio Merge Universal Viewer Merge Hemo Model RCSV2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LLZ	System, Image Processing, Radiological	Radiology	Class 2	892.2050	2011-11-21
DQK	Computer, Diagnostic, Programmable	Cardiovascular	Class 2	870.1425	2016-12-22
NFJ	System, Image Management, Ophthalmic	Radiology	Class 2	892.2050	2011-11-21
LLZ	System, Image Processing, Radiological	Radiology	Class 2	892.2050	2019-11-25
LLZ	System, Image Processing, Radiological	Radiology	Class 2	892.2050	2011-11-21
HWT	Template	Orthopedic	Class 1	888.4800	2018-01-15
LLZ	System, Image Processing, Radiological	Radiology	Class 2	892.2050	2010-06-22
LLZ	System, Image Processing, Radiological	Radiology	Class 2	892.2050	2025-07-30
DQK	Computer, Diagnostic, Programmable	Cardiovascular	Class 2	870.1425	2024-06-28

Official Correspondent

Nadia Marchant

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Merge Healthcare

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3032014234	Merge Canada	Mississauga Ontario, CA

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K080013	Agfa Healthcare Corporation	REGISTRATION AND FUSION	2008-01-17
K042221	Barco NV Barcoview	CORONIS 5MP MEDICAL FLAT PANEL DISPLAY SYSTEM	2004-12-30
K092915	Cedara Software Corp.	CEDARA WEBACCESS, MODEL: 2.4	2010-06-23
K961871	Siemens Medical Solutions USA, Inc.	FLOUROSPOT T.O.P.	1996-07-31
K122260	Aycan Digitalsysteme GmbH	AYCAN MOBILE	2012-09-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0012-2022	GE Healthcare, LLC	2	Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
Z-0023-2016	GE Healthcare	2	Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and displayed within the system or across computer networks at distributed locations.
Z-0030-2026	CHANGE HEALTHCARE CANADA COMPANY	2	Change Healthcare Radiology Solutions software version 14.2.2
Z-0032-2012	Philips Healthcare Inc.	2	MDC PACS - release R2.3 SP1 . Phillips Healthcare Andover, Massachusetts A software application that is used for receiving, managing, archiving, distributing and recording medical images onto portable digital media (including but not limited to Compact Disk and DVD).
Z-0033-2007	AGFA Corp.	2	IMPAX 5.2 Systems with CAD Capability (Computer Assisted Diagnosis)

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3010956703	Visual Medica	Ciudad Autonoma Buenos Aires Buenos Aires, Ciudad Autonoma de, AR
3030088963	REBRAIN	PESSAC Gironde, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183926. Last updated year: 2026. Please use registration number 2183926 when referencing this establishment in official correspondence.