3Derm Systems, Inc. (3Derm), a leader in the skin imaging and diagnostics industry, announced today that it has been granted two FDA Breakthrough Device designations for 3DermSpot, an algorithm that uses artificial intelligence (AI) and highly standardized skin images to autonomously detect melanoma, squamous cell carcinoma, and basal cell carcinoma.
BOSTON, Jan. 7, 2020 /PRNewswire/ -- 3Derm Systems, Inc. (3Derm), a leader in the skin imaging and diagnostics industry, announced today that it has been granted two FDA Breakthrough Device designations for 3DermSpot, an algorithm that uses artificial intelligence (AI) and highly standardized skin images to autonomously detect melanoma, squamous cell carcinoma, and basal cell carcinoma. 3Derm demonstrated its potential to provide a more effective diagnosis for life-threatening and irreversibly debilitating diseases to qualify for this fast-track program. 3DermSpot is the first autonomous AI device in the dermatology space to receive Breakthrough designation, joining only one other autonomous AI device. If ultimately approved by the FDA, 3DermSpot will be the first to bring dermatologist-level triage to primary care. Autonomous AI Makes Sense for Frontline Care Building Responsible AI Takes a Village The key to avoiding common AI pitfalls is close collaboration with all corners of the medical community. "We're operating in a field with a lot of snake oil. To get this right, we must hold ourselves to a higher clinical standard and continuously incorporate the perspectives of patients, providers, and regulators," said Liz Asai, CEO and Co-Founder of 3Derm. "We are thrilled to receive these Breakthrough designations and to have additional support in our ongoing regulatory discussions." 3DermSpot Addresses a Serious Public Health Issue About 3Derm Systems, Inc. Elektra Alivisatos, Director of Commercial Operations
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