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Year

04/01/21

Neuronetics Announces Appointment of Robert Cascella to its Board of Directors

03/11/21

Neuronetics Announces Retirement of Gregory Harper, Vice President, R&D and Clinical

03/09/21

Neuronetics Enhances TrakStar® Cloud Patient Data Management System to Maximize Physician Efficiencies

03/03/21

Neuronetics Names Cory Anderson Vice President, Clinical Affairs and Medical Operations

03/02/21

Neuronetics Reports Fourth Quarter and Full Year 2020 Financial and Operating Results

02/23/21

NeuroStar® Advanced Therapy Outcomes Registry Clinical Data Published in Brain Stimulation Validates Depression Treatment Protocols

02/16/21

Neuronetics to Report Fourth Quarter and Fiscal Year 2020 Financial and Operating Results and Host Conference Call

02/11/21

Neuronetics Announces Strategic Leadership Promotions to Support Future Growth

02/10/21

Neuronetics to Participate at the BTIG Virtual MedTech, Digital Health, Life Science & Diagnostic Tools Conference

02/02/21

Neuronetics Announces Closing of Public Offering and Exercise in Full of the Underwriters’ Option to Purchase Additional Shares

01/28/21

Neuronetics Announces Pricing of $75 Million Public Offering of Common Stock

01/28/21

Neuronetics Announces Proposed Public Offering of Common Stock

01/19/21

NeuroStar® Advanced Therapy’s Depression Outcomes Registry Hits 10,000 Patient Milestone

01/12/21

Neuronetics Reports Preliminary Fourth Quarter and Fiscal Year 2020 Financial Results

01/07/21

Neuronetics to Participate at the 23rd Annual ICR Westwicke Conference

01/07/21

Neuronetics Announces Expansion of Sales Organization

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Indication

NeuroStar TMS Therapy is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to receive satisfactory improvement from prior antidepressant medication in the current episode.

NeuroStar TMS Therapy is only available by prescription. A doctor can help decide if NeuroStar TMS Therapy is right for you.

Important Safety Information

The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of NeuroStar TMS (<0.1% per patient).

NeuroStar TMS Therapy should not be used with patients who have non-removable conductive metal in or near the head. NeuroStar TMS Therapy has not been studied in patients who have not received prior antidepressant treatment.
Safety and Prescribing Information »

Our Commitment

Neuronetics is committed to compliance with state and federal laws regarding interaction with healthcare providers.
Commitment to Compliance »

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