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NeuroOne Medical Technologies Corporation Initiates Limited Commercial Launch of OneRF Ablation System
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NeuroOne Medical Technologies Corporation Reports Earnings Results for the Full Year Ended September 30, 2023
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NeuroOne Gets FDA Clearance to Market OneRF Ablation System; Shares Fall
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NeuroOne Medical Technologies Corporation Receives FDA 510(K) Clearance to Market its OneRF(TM) Ablation System
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NeuroOne Medical Technologies Gets Notice of Allowance for Drug Delivery Patent
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NeuroOne Medical Technologies Corporation Announces Patent Allowance for Drug Delivery Utilizing a Novel Neural Probe
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NeuroOne Medical Technologies Corporation Provides Progress Update on FDA 510(k) Submission for OneRF?? Ablation System
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NeuroOne Medical Technologies Corporation Reports Earnings Results for the Third Quarter and Nine Months Ended June 30, 2023
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NeuroOne Medical Technologies Corporation Submits 510(K) Application to FDA for OneRF™ Ablation System
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NeuroOne Medical Technologies Corporation Announces First Clinical Case Using Evo® sEEG Electrode in Robotic Neurosurgery
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NeuroOne Medical Technologies Corporation Reports Earnings Results for the Second Quarter and Six Months Ended March 31, 2023
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NeuroOne® Successfully Completes Initial Animal Implant of Novel Thin Film Paddle Lead for Spinal Cord Stimulation
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NeuroOne Medical Technologies Gets US Patent for Thin Film Electrode Technology
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NeuroOne Medical Technologies Corporation Awards U.S. Patent Covering Novel and Proprietary Thin Film Electrode Platform
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NeuroOne Medical Technologies Corporation Reports Earnings Results for the First Quarter Ended December 31, 2022
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NeuroOne Medical Technologies Corporation Reports Earnings Results for the Full Year Ended September 30, 2022
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NeuroOne Successfully Completes Feasibility Study with its OneRF Ablation System
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NeuroOne Says it Shipped First Electrode Device Order to Zimmer Biomet
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NeuroOne Medical Technologies Corporation Ships First Commercial Order to Zimmer Biomet
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NeuroOne Medical Technologies Corporation Receives U.S. Food and Drug Administration 510(K) Clearance to Market Its Evo sEEG System for Less Than 30 Day Use
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