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Japanese Startup AI Medical Secures FDA Approval for Real-Time Endoscopic AI Platform

by Fred Pennic 11/11/2019 Leave a Comment

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Japanese Startup AI Medical Secures FDA Approval for Real-Time Endoscopic AI Platform

Key Highlights

– AI Medical Service, a Toyoko, Japan-based endoscopic artificial intelligence provider announces it has been granted Breakthrough Device Designation by the FDA.

– FDA Breakthrough Device Designation expedites the traditional development, assessment, and review process, and enables medical professionals to get access to new developments quickly.

– Designation will also enable the company to launch its project in the U.S. and expand to other markets across the world.

AI Medical Service Inc., one of the world’s first real-time endoscopic artificial intelligence (AI) developers, today announced the Company has secured Breakthrough Device Designation by the U.S. Food and Drug Administration (FDA) for its AI programs that analyze endoscopy images for potential diagnosis of gastric cancer.  This designation will be critical as the company continues to accelerate clinical and regulatory program especially in terms of prioritized review of the submission.  At the same time as obtaining approval in its original country, Japan, the Company will continue to work through the regulatory process in the United States and other countries, and move on to global expansion.

Why The FDA Breakthrough Device Designation Matters

Breakthrough Device Designation is granted to medical devices and device-led combination products that provide the potential for a more effective treatment option for life-threatening or irreversibly debilitating diseases. It expedites the traditional development, assessment and review process, and enables medical professionals to get access to new developments quickly.

AI Medical Service’s system applies neural network algorithms which are trained with large real-world datasets of images of biopsy-proven cancer lesions, benign lesions, and normal tissue that was captured using standard endoscopes, thus aiding physicians performing endoscopies to detect lesions suspicious for cancer. AI Medical’s technology is further differentiated as it is able to detect gastric, colorectal, and esophageal cancer, especially for concurrent usage whereas other entities’ technology tends to focus only on colorectal cancer.

Recent Traction & Research Results

To date, AI Medical Service, Inc. collaborates with approximately 80 medical institutions representing Japan in the field of gastrointestinal endoscopy to research and develop AI endoscopies. The results have been widely accepted by experts all over the world, including the conference for Digestive Disease Week (DDW), the world’s largest gastroenterology association, in which as many as 12 studies by AI Medical Service was selected for the presentation including the one awarded as “Best of DDW.” The company will enable the practical use of these technologies at an early stage and will contribute to the world’s endoscopic medical practice by supporting physicians’ diagnoses, thereby reducing the risk of overlooking diseases to the highest extent possible.

In addition, the company raised 42.9M in Series B funding from Globis Capital Partners, World Innovation Lab (WiL) and Sony Innovation Fund by IGV (Innovation Growth Ventures), as well as additional third-party allocations. Following the last funding round in August 2018 of over $9M from the Incubate Fund, this brings the company to approximately $57M raised since its founding in 2017.

“We will launch this groundbreaking technology approved by the FDA as soon as possible in the US market.  As our founding philosophy states, we plan to contribute to endoscopic medical treatment around the world,” said Dr. Tomohiro Tada, CEO of AI Medical Services.

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Tagged With: AI, algorithms, Artificial Intelligence, cancer, Endoscopy, FDA, Medical Devices, Partners, physicians, risk

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