• JLK has secured FDA 510(k) clearance for JLK-PWI, an AI-based solution for analyzing brain MR perfusion images to detect brain infarction areas, marking their fourth FDA approval this year.
• A study by Chonnam National University Hospital showed JLK-PWI had a significantly lower lesion detection failure rate (1.9%) in stroke patients compared to Rapid AI (61.4%).
• JLK plans to leverage this FDA approval to expand its presence in the U.S. AI healthcare market, which constitutes 59% of the global market, and aims to become a comprehensive stroke solution provider.
• With recent funding of 49 billion won, JLK intends to pursue FDA approval for three additional stroke solutions, further solidifying its portfolio of AI-driven medical technologies.