AI reveals image detail. Supporting clinical judgment.
FOUR CORE ANALYSES
SPINAL STENOSIS
AI segments the dural sac and measures its diameter to show differences across lumbar levels. Comparing the original images with the measurements helps physicians identify the location and extent of narrowing and assess compression.
BUILT AROUND YOUR WORKFLOW
Connect image import, AI analysis and physician review, bringing quantitative findings into interpretation and reporting at each step of the clinical workflow.
REGULATORY & CLINICAL EVIDENCE
Clinical research and adherence to medical device regulations and standards provide evidence for analytical accuracy and a foundation for trusted clinical innovation.
TFDA · TAIWAN
Taiwan Class II medical device clearance for the AI-based quantitative spine MRI analysis system.
Taiwan medical device manufacturing license No. 008564CE · EUROPE
CE marking provides a regulatory basis for use in the European Union market.
European Union | CECLINICAL STUDY
The functional validation study received IRB approval and institutional authorization from Taipei Veterans General Hospital, enabling clinical validation under research ethics requirements.
IRB: 2024-08-008C · 12 Sep 2024PUBLICATION
Research on automated lumbar MRI segmentation and quantitative assessment was published in Neurospine in 2024, presenting the technical methods and analysis performance in a peer-reviewed journal.
Read the research paper
Clinical implementation | Seoul, South Korea
Working with Dr. Kim Hyun-sung’s team, we deployed an in-hospital AI imaging analysis service to support pre- and postoperative lumbar assessment. Quantitative information complements clinical interpretation and extends the role of imaging analysis in patient care.
Research collaboration | Seongnam, South Korea
In collaboration with Dr. Han In-bum’s team, we are researching AI-based quantitative assessment of recovery after lumbar fusion. By combining medical imaging analysis with clinical research needs, the project explores the potential of quantitative imaging indicators in postoperative assessment.
Medical device clearance, research ethics approval and journal publication each have a distinct scope. Product use is governed by the approved labeling.
FAQ
Answers to common questions about product capabilities and clinical implementation.
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This page presents product analysis examples. Results support interpretation by medical professionals and must be assessed alongside the original images and clinical information.
