Pivotal U.S. Investigational Device Exemption (IDE) cleared trial
PURSUIT is a randomized, double-blinded, sham-controlled, IDE-cleared trial that enrolled 415 subjects with moderate SUI at approximately 30 study sites in the United States. Subjects were randomized in a 2:1 ratio to the active Viveve treatment or an inert sham treatment.
Viveve aspires to be the leader
in the treatment of female
Stress Urinary Incontinence
The internationally patented Viveve® System incorporates Cryogen-cooled Monopolar Radiofrequency (CMRF) technology to uniformly provide an endovaginal treatment that is non-ablative.

The Viveve Leadership Team
The Viveve leadership team is an experienced group of individuals dedicated to upholding our values and achieving our vision and mission.
Meet the Senior Leadership TeamViveve Career Opportunities
The Viveve team is dedicated to working together to find innovative, non-invasive products for female Stress Urinary Incontinence. Learn about our culture.
Explore Career Opportunities