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Moon Surgical’s Maestro System has received FDA clearance for its commercial version and CE mark in Europe. The system has been used in over 1,100 patients across the US and Europe as of March 2025. Clinical use spans general, bariatric, gynecologic and urologic surgeries. The company’s ScoPilot AI feature was the first FDA-cleared AI-driven intraoperative movement control on a robotic platform. Early clinical experience demonstrates enhanced surgeon autonomy and workflow efficiency.
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