General Vibronics, Inc. is a U.S. medical device company advancing cold atmospheric plasma science for clinical applications worldwide.

The MIRARI® Cold Plasma System designed and manufactured by General Vibronics, received U.S. FDA clearance, establishing it as a Class II medical device authorized for U.S. market distribution.
General Vibronics, Inc. is a medical device company headquartered in Tempe, Arizona. We design, develop, and commercialize cold atmospheric plasma therapeutic devices, providing healthcare professionals with an FDA 510(k) Cleared, non-invasive treatment modality.
Our flagship product, the MIRARI® Cold Plasma System, is the result of years of research at the intersection of plasma physics, biomedical engineering, and clinical medicine. It is cleared by the U.S. FDA, approved by the Thai FDA, and registered with the Vietnam Ministry of Health.
About General Vibronics
An FDA-cleared, handheld therapeutic platform that utilizes Dielectric Barrier Discharge (DBD) technology with 80 kHz monopolar radiofrequency energy. The MIRARI® is indicated for heating for the purpose of elevating tissue temperature for selected medical conditions such as temporary relief of pain, muscle spasms and increase in local circulation.
U.S. FDA
510(k) Cleared (Class II)
Thai FDA
Approved & Registered
Vietnam MOH
Registered Medical Device
ISO 13485:2016
Certified QMS
Journal of Wound Care (JWC)
World Union of Wound Healing Societies (WUWHS)