Vitrea

Vitrea® is a medical diagnostic system that allows the processing, review, analysis, communication and media interchange of digital images acquired from a variety of imaging devices. Vitrea…

Registry build 21.09.26

Vitrea® is a medical diagnostic system that allows the processing, review, analysis, communication and media interchange of digital images acquired from a variety of imaging devices. Vitrea is not meant for primary image interpretation in mammography. Vitrea provides visualization of digital images to aid clinicians in their analysis of anatomy and pathology. The Vitrea user interface follows typical clinical workflow patterns to process, review, and analyze digital images. It is a web-based imaging system that allows physicians to use PCs or notebook computers to remotely access to 2D and 3D advanced visualization using a Microsoft web-enabled browser. Vitrea modules include automated and semi-automated visualization and advanced quantification tools targeted for a specific study based on a protocol selected by the user. The automation is only intended to reduce the manual steps required by the user to analyze and quantify the data from the images; it is not intended to detect pathology or disease. The software provides imaging information as an assist to the physician.

8manufacturers in China registered for this device type
4catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (2), Shanghai (2), Jiangsu (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JAK
Manufacturer City Province Registered as Device types
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shanghai, Medical Equipment Ltd. Shanghai Shanghai Contract manufacturer 10
Neusoft Medical Systems Co., Ltd. Shenyang Liaoning Manufacturer 1
Philips Health Technology (China) Co., Ltd. Shenyang Branch Shenyang Liaoning Specification developer 1

Record

Regulatory record for Vitrea
Listed by Canon Medical Informatics, Inc., United States
FDA product code JAK
Device type System, X-Ray, Tomography, Computed
Device class Class 2
Regulation 21 CFR 892.1750
Establishment Repacker / relabeller, Manufacturer, Exporter
510(k) K032748
Record published 2016-12-22
Record revised 2023-10-18 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Vitrea
Catalogue number Size Status
7.3.2 In distribution
7.3.1 In distribution
6.9.2 In distribution
6.9 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Visicoil IZI Medical Products LLC 48
Visicoil MR IZI Medical Products LLC 41
Illumisite Covidien LP 25
Imbio LDA Imbio, LLC 24
Edge Covidien LP 20
Revolution GE Hangwei Medical Systems Co., Ltd. 20
Gold Fiducial IZI Medical Products LLC 20
superDimension Covidien LP 17
Lodox Lodox Systems (PTY) Ltd. 12
Revolution GE Medical Systems, L.L.C. 12
Toshiba Scanner Canon Inc. 10
syngo.CT Dual Energy Siemens Healthcare Limited 7

Showing 12 of 495. All products under System, X-Ray, Tomography, Computed

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252217 2025-11-28
K243240 2025-04-10
K223261 2023-07-13

Recalls Naming This Product

8 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Vitrea
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Canon Medical Informatics, Inc. 510(k) number 2013-10-21 Class II Software design Vital Images, Inc. has found an issue in VitreaCore software though internal testing. There is a potential for incorrect and possibly reversed image orientation for certain snapshots taken in VitreaCore software versions 6.0, 6.1, 6.2, 6.3 598 2015-01-16
Canon Medical Informatics, Inc. 510(k) number 2013-03-15 Class II Software design Vital Images has made a decision to perform a field correction to the Vitrea CT Multi-Chamber Cardiac Functional Analysis application. Vital Images has identified a defect in which numerical values may be incorrect in the Results Table unde 102 2015-02-27
Canon Medical Informatics, Inc. 510(k) number 2013-03-15 Class II Labeling design Vital Images, Inc. (Vital Images) received one report about potential user confusion when viewing a brain perfusion scan on Vitrea CT Brain Perfusion 2D when the scan was performed using a wide coverage shuttle acquisition technique. This 1,978 2015-04-08
Canon Medical Informatics, Inc. 510(k) number 2012-08-13 Class II Software design Vital Images has found two potential errors in calcium score values in restored snapshots of studies generated through use of Vitrea or Vitrea Enterprise Suite. This issue affects Version 3.1 of Vitrea fX; Version 5.2 of Vitrea; Versions 6 2088 (1133 USA) 2015-03-25
Canon Medical Informatics, Inc. 510(k) number 2011-11-11 Not classified Software design Vital Images has found two issues that may display incorrect Standard Update Values (SUV) when viewing certain PET/CT images. This issue affects the VitreaCore PET/CT feature for Vitrea Enterprise Suite 1.2, 1.3, 6.0, 6.1, including all up 338 (233 US) 2013-12-03
Canon Medical Informatics, Inc. 510(k) number 2010-10-14 Not classified Software design Vital Images Inc., reported that a software defect exists with Vitrea fX 2.1, 3.0 and 3.1 CT Brain Analysis whereby the annotated numeric ROI values on a batched perfusion map are incorrect when created using the auto batching function (fro 182 2012-05-15
Canon Medical Informatics, Inc. 510(k) number 2010-08-23 Not classified Software design There is a potential alignment error of fused PET/CT images in the Vitrea Core component of Vitrea Enterprise Suite 1.2 and 1.3. The error occurs during panning of the fused PET/CT images. Because the PET data has a larger voxel size than 178 2012-11-06
Canon Medical Informatics, Inc. 510(k) number 2007-11-08 Not classified Process control Standard Uptake Values (SUV) display/update problems; in the way Standard Uptake Values (SUV) are displayed in 3D/MPR views. The problem arises when a user draws a selected region of interest in order to calculate the SUV statistics of the 18 2011-12-17

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer