Publications
Our commitment to advancing surgical robotics is supported by peer-reviewed clinical evidence across our technology platforms. Geniant® Cranial received FDA clearance in January 2025 and is marketed in the United States. Research from our predecessor system, which received MFDS approval in July 2016 and is marketed in South Korea, is included below for reference.
Year
Title
Authors
Link
2025
Safety and efficacy of stereoelectroencephalography using a novel robot based on the center-of-arc principle in patients with medically refractory epilepsy
Year
2025
Title
Safety and efficacy of stereoelectroencephalography using a novel robot based on the center-of-arc principle in patients with medically refractory epilepsy
Authors
Link
Contact
geniant@kohyoung.com
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San Diego, CA 92128 USA