医療従事者の為の最新医療ニュースや様々な情報・ツールを提供する医療総合サイト

Heuron Gets FDA Green Light for Stroke Triage and Notification Solution

2024年05月24日 AM05:13
このエントリーをはてなブックマークに追加


 

SAN JOSE, Calif.

Heuron, a specialized medical AI startup focused on brain and neurological disorders based in South Korea, announced that its non-contrast CT imaging analysis solution, Heuron ICH, has received FDA 510(k) clearance. This marks the first FDA approval of an AI-based brain disorder analysis solution from Korea for computer-aided triage and notification devices (CADt).

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20240523049704/en/

Heuron ICH Worklist (Graphic: Business Wire)

Heuron ICH Worklist (Graphic: Business Wire)

Heuron ICH is an advanced AI solution designed to automatically screen and signal potential cases of intracranial hemorrhage, relying solely on non-contrast CT images. Its primary function is to swiftly discern emergency brain hemorrhages that require immediate attention, even capturing the minutest hemorrhages that often elude human detection. Notably, Heuron ICH boasts a sensitivity of 86% and specificity of 88%, ensuring reliable and accurate assistance in critical medical scenarios.

Heuron ICH becomes the fifth solution from Heuron to receive FDA clearance, following Veuron-Brain-mN1, Veuron-Brain-pAb, Heuron Beta Amyloid, and Veuron-Brain-pAb3. Currently, Heuron holds 15 domestic medical device approvals/certifications, four European CE (MDD) certifications, and various other international certifications.

Donghoon Shin, CEO of Heuron, expressed, “Securing this product approval marks a significant milestone, facilitating our swift penetration into the U.S. market. Our commitment extends beyond this achievement as we endeavor to expand our portfolio of FDA-approved medical solutions. We are dedicated to optimizing the utilization of Heuron’s diverse offerings within U.S. clinical environments, particularly for emergency patient care.”

Additionally, Heuron ICH successfully achieved the performance levels required by the FDA through clinical trials conducted last year in collaboration with Mass General Brigham, affiliated with Harvard Medical School.

About Heuron

Heuron Co., Ltd., founded in 2017, pioneers medical AI solutions for neurodegenerative diseases and emergency stroke care. Heuron’s cutting-edge software aids precise diagnosis of conditions like Alzheimer’s and Parkinson’s disease while expediting stroke treatment through the StroCare Suite™. Collaborating globally, Heuron strive to enhance brain health through AI-driven diagnostics, addressing challenges posed by aging populations. For more information, please visit: https://iheuron.com/en/

View source version on businesswire.com: https://www.businesswire.com/news/home/20240523049704/en/

CONTACT

Eunsil Kang

Chief Strategy Officer

christina.kang@iheuron.com, heuron@iheuron.com

同じカテゴリーの記事 

  • 卫材启用Medidata Clinical Data Studio推进临床试验效率和患者体验的革新
  • Fujirebio推出研究专用全自动Lumipulse®G GFAP检测试剂盒并进一步强化该公司的神经病学产品阵容
  • Fujirebio Launches the Fully Automated Lumipulse® G GFAP Assay for Research Use Only and Further Strengthens its Neuro Test Menu
  • Pearl、歯科AIで史上最大5,800万ドルの資金調達ラウンドを実施
  • FIGS Announces Date of Second Quarter 2024 Earnings Release, Conference Call and Webcast