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CONTACT US

GET YOUR INDIVIDUAL OFFER


The offer is available at all SEBERS Medical offices. Further attractive offers are available from your authorized SEBERS Medical distributor. Contact us today for more information.

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CONTACT OUR TEAM

At SEBERS Medical, we are committed to finding the right solutions for our customers by continually advancing our technology and expanding our global reach. Our dedication to innovation drives us to develop TMS devices that not only meet but exceed industry standards. We prioritize understanding the unique needs of our clients, ensuring that our products deliver exceptional performance and reliability. By partnering with leading experts and distributors worldwide, we strive to make cutting-edge brain stimulation solutions accessible to a broader audience, ultimately enhancing the well-being of individuals everywhere. 

What is TMS?

Repetitive Transcranial Magnetic Stimulation (TMS) is a non-invasive technology (applied with a TMS device) of brain stimulation in which an electric current is induced in the brain by means of alternating magnetic fields. 

It is a treatment alternative for people suffering from e.g. major depressive disorder. TMS is typically used when other depression treatments have not been effective. 

This form of therapy is well tolerated and does not cause systemic side effects. It can be performed on an outpatient basis and does not require anesthesia.

 

CONTACT INFO

Phone: 833.3BUY.TMS (+1.833.3289.867)

Email: Sales@sebersmedical.com

Address: 230 S Broad Street, 17th Floor Philadelphia, PA 19102

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LEGAL

Disclaimer:

Regulations in the United States

*United States Federal Law regulates the sale of Medical Devices. The Blossom TMS Therapy System is indicated for the treatment of Major Depressive Disorder in adult patients, who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. (K220625) All other devices on this website are not approved and/or cleared for use in treatment and/or diagnosis in the United States. All investigational devices must be labeled in accordance with the labeling requirements of the IDE regulation (§ 812.5) and bear a label that states:
“CAUTION.
Investigational Device. Restricted by federal (or United States) law to research use.”