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Home » Magstim earns FDA clearance for transcranial magnetic stimulation that treats depression, OCD

Magstim earns FDA clearance for transcranial magnetic stimulation that treats depression, OCD

November 12, 2024 By Sean Whooley

Magstim Horizon Inspire TMS (1)
The Horizon Inspire System. [Image courtesy of Magstim]
Magstim announced today that the FDA cleared its next-generation Horizon Inspire system for delivering transcranial magnetic stimulation (TMS).

Clearance paves the way for the use of the TMS technology to treat patients with major depressive disorder (MDD), obsessive-compulsive disorder (OCD) and anxious depression.

Minneapolis-based Magstim designed Horizon Inspire to address physician needs with high-power air cooling and the ability to deliver back-to-back customizable treatments. It offers ease of use, cost-effectiveness and portability between clinic rooms.

The company built Horizon Inspire on its Magstim TMS technology, which has prior FDA clearances. It leverages intuitive preset clinical workflows to simplify the treatment process. Magstim says its system delivers precise results with no pulse decay, ensuring the correct dosage. The air-cooled coil reduces downtime and eliminates additional cooling expenses, while advanced data analytics tools improve treatment efficacy.

“Physicians, nurse practitioners and mental health care professionals tell us that patients are searching for alternatives to pharmaceutical treatments,” said Ronnie Stolec-Campo, CEO, Magstim. “FDA cleared transcranial magnetic stimulation is a proven and effective treatment with minimal side effects. We designed the Inspire to enable both experienced TMS providers as well as those who are new to TMS.”

“Magstim engineered the very first commercially available TMS research technology, and we remain committed to our foundation of research. We are unique in the industry because we do not charge pay per use fees, we maintain a dedicated service and support team, and we manufacture our own technology.”

Filed Under: 510(k), Bioelectronic Medicine, Featured, Food & Drug Administration (FDA), Health Technology, Neurological, Neuromodulation/Neurostimulation, Regulatory/Compliance, Software / IT Tagged With: magstim

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About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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