Vieworks Co., Ltd.

FDA Device Registration & Listing · Hwaseong-si Gyeonggi, KR · Registration 3017585294

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
3017585294
FEI Number
3017585294
Entity Name
Vieworks Co., Ltd.
City/State/Country
Hwaseong-si Gyeonggi, KR
Establishment Address
25-7, Jeongnamsandan 2-gil, Jeongnam-myeon, Hwaseong-si Gyeonggi 18514, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Vieworks Co., Ltd. (Owner Number: 10024523)
Owner / Operator Contact Address
41-3, Burim-ro 170beon-gil, Dongan-gu, Anyang-si, KR-41 14055, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VIVIX-S 4386W Cuattro ONE L8643-AWV Saturn 8000 VIVIX-S F series F3025-AW VIVIX-S FW VIVIX-S 1717V Saturn 8000 VIVIX-M VXvue VIVIX-S 1717N Saturn 8000 ViVIX-S Wireless PRO 3543 PRO 3543C Saturn 8000 QXLink VXvue PRO 3543T PRO 3543TC PRO 4343FC PRO 4343F Saturn 8000 ViVIX-S

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2022-09-14
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2022-07-21
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2018-05-16
MUE Full Field Digital, System, X-Ray, Mammographic Radiology Class 2 892.1715 2025-01-17
LLZ System, Image Processing, Radiological Radiology Class 2 892.2050 2026-04-02
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2016-03-02
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2013-02-14
LLZ System, Image Processing, Radiological Radiology Class 2 892.2050 2016-08-11
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager) Radiology Class 2 892.1680 2013-01-19

Official Correspondent

Serin Park

US Agent Details

Peter Lee Business: Vieworks America Ltd. Email: regulatory.us@vieworks.com Phone: (714) 6134338

Related Public Records

Same Entity

Vieworks Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3006013411 VIEWORKS CO., LTD. Anyang-si Gyeonggi, KR

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K070563 Vidar Systems Corp. VIDAR VISION 2000 2007-03-16
K190691 Pixxgen Corporation Pixx2430 Digital Diagnostic X-Ray Receptor Panel 2019-04-04
K150150 Rayence Co., Ltd. 1717SGN / 1717SCN Digital Flat Panel X-ray Detector 2015-03-27
K140771 Philips Medical Systems Dmc GmbH PHILIPS ELEVA WORKSPOT 2014-04-25
K080013 Agfa Healthcare Corporation REGISTRATION AND FUSION 2008-01-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2009 Toshiba American Medical Systems Inc 2
Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography System with version 3.40 or higher software. Controller for Infinix interventional angiography systems.
Z-0031-2007 AGFA Corp. 2
CR DX-S, Image Intensified Fluoroscopic X-ray system.
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017585294. Last updated year: 2026. Please use registration number 3017585294 when referencing this establishment in official correspondence.
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