USA

!!!ATTENTION CUSTOMERS!!!

SCENAR™ devices are Class IIa medical devices and their import, use, maintenance and training are controlled by the U.S. Food and Drug Administration (FDA).  These devices can only be purchased from a registered FDA Company.

In USA, SCENAR™ devices can be sold to medical practitioners only or to patients by prescription.

Authorised Distributor for RITM SCENAR™ products and Registered in FDA:

Scenar Health USA LLC
2620 Regatta Drive Suite 102
Las Vegas NV 89128
Toll Free: (800) 680-6394
Phone: (702) 553-1080
Fax: (702) 537-5290
Email: info@scenarhealth.us
web: www.scenarhealth.us