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Revolutionize Therapy with the Blossom TMS™ Therapy System

BLOSSOM TMS™ THERAPY SYSTEM

Blossom TMS is an FDA-cleared non-invasive, non-drug treatment for patients suffering from depression who are dissatisfied with the effectiveness of antidepressants*
Blossom TMS Therapy System

Why Blossom TMS?

  • Device Plugs Into Standard 120V USA electrical outlets
  • No pay-per-use or costly disposables
  • Industry leading coil cooling
  • $62,500 Starting Price
  • Training Included
  • Utilizes Blossom ‘Quiet Coil’

Lock in our $49,500
promotional online offer today

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SPECS

Personalized TMS Therapy Experience

Give your TMS system a personal touch. Adapt the appearance of your Blossom TMS™ Chair to your needs. Choose from a variety of colors and materials to match your clinic's aesthetic. Enhance patient comfort and satisfaction with a chair tailored to your specifications.

Reliable and Efficient TMS Solutions

The Blossom TMS Therapy system is engineered for clinical efficiency. Built from the ground up for clinical use, it offers reliable and consistent performance, allowing for seamless back-to-back treatment sessions.

Effective Treatment for Major Depressive Disorder

The Blossom TMS Therapy System is indicated for the treatment of Major Depressive Disorder in adult patients, who have failed to achieve satisfactory improvements from prior antidepressant medication.*

TESTIMONIALS


Make Depression Therapy easy with the Blossom TMS™ System.

HEADNEST™
CHAIR
TREATMENT

CONTACT INFO

Phone: 833.3BUY.TMS (+1.833.3289.867)

Email: Sales@sebersmedical.com

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

QUICK LINKS

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.”