visor2™ — Smart Neuronavigation for TMS
Bring more confidence and consistency to personalized TMS treatments with FDA 510(k) cleared neuronavigation, precise optical tracking, and a workflow designed for everyday clinical use.
*visor2™ is an FDA 510(k)-cleared* neuronavigation solution for clinical applications, providing precise and accurate positioning of TMS coils for personalized treatments, supporting clinicians in delivering optimal patient care.
Precise and Consistent Targeting
Help your clinic deliver TMS pulses with greater precision and reproducibility using guided coil positioning and advanced optical tracking.
Assisted Motor Threshold and Mapping
Facilitates motor threshold determination with enhanced motor mapping functions and a flexible number of EMG channels.
Built around your clinic's workflow
Choose the targeting workflow that fits your clinic: from MRI-free planning to MRI- or fMRI-guided navigation. Flexible, adaptable solutions designed to support your evolving clinical needs.
Regulatory Confidence
FDA 510(k)-cleared* and manufactured by an ISO 13485 certified facility, ensuring confidence and compliance for clinical settings.

Designed for Personalized TMS Treatment
visor2 combines advanced optical tracking with individualized MRI guidance to deliver precise, patient-specific TMS targeting for consistent and personalized treatment.
Spotlight
Clinical Application of visor2 for Brain Stimulation
Hear from Dr. Rebecca Cohen and Dr. Jordana Hollen of Cohen & Associates on the clinical advantages of visor2.
Read the Showcase
Broad TMS Stimulator Compatibility
visor2 is compatible with the majority of FDA-cleared TMS stimulators from Neurostar, Neurocare, Magstim, Magventure, and others, fitting into existing clinical setups without disruption.
Contact UsReady to Elevate Your TMS Practice?
Get in touch with our experts to learn how visor2 fits your clinical workflow.
visor2™ system has FDA clearance under 510(k) in the USA, is CE marked medical device (CE Class IIa) under MDR (EU) 2017/745, Medical Device License (MDL) issued by Health Canada, and is registered in the ARTG in compliance with the Australian TG(MD)R.
EEG-TMS, tFUS and dual-coil navigation with visor2 is intended for research and educational use only.
Information intended for users in USA: Conditions that are FDA cleared for treatment with TMS are specific to each stimulation device. Please consult your stimulator manufacturer for more information.
Manufactured by eemagine Medical Imaging Solutions GmbH, Berlin, Germany, ISO 13485 certified. ANT Neuro and eemagine are part of the neuromotion group.
For more information about visor2 and the regulatory status in your country, contact us at sales@ant neuro.com.
