Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024689474

FEI Number

3024689474

Entity Name

Barco Inc Portland

City/State/Country

Portland, OR, US

Establishment Address

735 SW 20th Place, Suite 100, Portland, OR 97205, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BARCO NV (Owner Number: 9031117)

Owner / Operator Contact Address

Beneluxpark 21, Kortrijk, BE-VWV 8500, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K191845

PMA Number

N/A

All Registered Proprietary Names

MDCC-6530 Coronis Fusion 6MP Coronis Fusion 4MP Intuitive Workflow Tools (IWT) MDCC-4430

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PGY	Display, Diagnostic Radiology	Radiology	Class 2	892.2050	2019-09-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BARCO NV

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004578804	Barco, Inc	DULUTH, GA, US
3024137003	Barco (Suzhou) Healthcare Technology Co., Ltd.	Suzhou Jiangsu, CN
9613188	BARCO N.V.	KORTRIJK West-Vlaanderen, BE
1000181154	BARCO S.R.L.	Saronno Varese, IT

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K163335	Eizo Corporation	6MP Color LCD Monitor, RadiForce RX660, RX660-AR	2016-12-15

Similar Registrations

Registration Number	Establishment Name	Location
9613188	BARCO N.V.	KORTRIJK West-Vlaanderen, BE
3013084615	D&T INC.	Yuseong-gu Daejeon, KR
3024897454	TAURUS MEDICAL SOLUTIONS LTD	Cannock Staffordshire, GB
3000237660	EIZO CORPORATION	HAKUSAN Ishikawa, JP
3013501671	LG ELECTRONICS INC.	Gumi-si Gyeongbuk, KR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3024689474. Last updated year: 2026. Please use registration number 3024689474 when referencing this establishment in official correspondence.