Opulus Lymphoma Precision

Opulus Lymphoma Precision is software that segments and visualizes lesions in whole-body FDG-PET/CT scans of patients already diagnosed with FDG-avid lymphoma. It calculates total metabolic…

Registry build 21.09.26

Opulus Lymphoma Precision is software that segments and visualizes lesions in whole-body FDG-PET/CT scans of patients already diagnosed with FDG-avid lymphoma. It calculates total metabolic tumor volume from the segmented disease burden.

A machine learning algorithm identifies areas of tracer uptake and generates tumor-boundary regions and image overlays. Input consists of DICOM PET images with their associated attenuation-correction CT images.

Physician Review

The output assists trained interpreting physicians alongside standard image interpretation. A physician can accept or reject the generated result but cannot modify it. Radiologist review remains required; the software does not screen for or diagnose lymphoma.

8manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Beijing (4), Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code QIH
Manufacturer City Province Registered as Device types
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
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
Beijing Infervision Healthcare Medical Technology Co., Ltd. Beijing Beijing Complaint-file establishment 4
Wuhan United Imaging Healthcare Co., Ltd. Wuhan Hubei Manufacturer 4
Keya Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for Opulus Lymphoma Precision
Listed by Roche Molecular Systems, Inc., United States
FDA product code QIH
Device type Automated Radiological Image Processing Software
Device class Class 2
Regulation 21 CFR 892.2050
Establishment Specification developer, Manufacturer, Exporter
510(k) K243863
Record published 2026-05-08

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Opulus Lymphoma Precision
Catalogue number Size Status
10257873001 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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uOmnispace Shanghai United Imaging Healthcare Co., Ltd. 3
Scenium Siemens Medical Solutions USA, Inc. 3
syngo.MI General Siemens Medical Solutions USA, Inc. 3
Neosoma Dashboard Neosoma, Inc. 3
BriefCase-Quantification Aidoc Medical Ltd. 3
OrthoNext™ Platform System Software Orthofix SRL 3
MI View&GO Siemens Medical Solutions USA, Inc. 3
FEops Feops NV 3
AI-Rad Companion Brain MR Siemens Healthcare Limited 3

Showing 12 of 147. All products under Automated Radiological Image Processing Software

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243863 2025-05-30

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