Precise targeting for TMS
Precise targeting for TMS treatment
ANT Neuro's FDA cleared visor2* TMS Neuronavigation system allows clinicians to deliver accurate, consistent, and personalized TMS sessions
Discover the power of visor2™ today
ANT Neuro's FDA cleared visor2 TMS Neuronavigation system allows to deliver more accurate, consistent, and personalized navigated TMS therapy
Best in class TMS Neuronavigation
Streamlined motor threshold determination, and precise, reproducible targeting of TMS pulses
targeting of TMS pulses.
The optional motor threshold measurement workflow in visor2™ facilitates fast and accurate measurement of a patient's motor threshold.
visor2's™ target helper tool guides the clinician to precisely place the TMS coil over user-defined treatment targets.
targets.
measurement workflow in visor2 facilitates fast and accurate measurement of a patient's motor threshold.
Personalized navigation with or without individual MRI or fMRI
visor2™* enables TMS providers to use an individual patient's brain image (MRI) or functional evaluation (fMRI) to define treatment targets and navigate the TMS coil based on the patient's unique neuroanatomy.
When a patient's MRI is unavailable a simple scalp-based navigation workflow using the 5.5cm rule guides placement of the TMS coil.
Compatible with most FDA 510(k) approved TMS systems
visor2™ seamlessly integrates with a wide range of TMS systems, including Magstim (Horizon), MagVenture, neurocare (Apollo), and Neuronetics (Neurostar). This open approach ensures that the visor2™ system will be compatible with your current TMS device without locking you in to a particular system.
Reusable tracking tools allow integration into your existing TMS setups with no recurring costs.
Checkout even more inspiring customer showcases,
publications and webinars at www.ant-neuro.com
Discover the power of visor2™ today
*Each TMS device is FDA cleared for specific indications. Please consult your TMS stimulator manufacturer for more information.
visor2™ system is CE marked as a medical device in the EU, class IIa and has FDA clearance under 510(k) in the USA. Medical Device License (MDL) issued by Health Canada. Compliant with the Australian TG(MD)R and registered in the ARTG. Manufactured by eemagine GmbH, Berlin, Germany, ISO 13485 certified. ANT Neuro and eemagine are part of the neuromotion group.