A Long-term Evaluation of a Novel Intravaginal Device

To determine the long-term clinical efficacy of the vSculpt therapy on treating the pelvic
floor area and vaginal tissue for females who experience bladder and sexual dysfunction.

Inclusion Criteria:

- All study participants are required to be biological females (genotype XX) to
participate

- Female participants will be of adult age, over 18

- Female participants with self-reported concerns with bladder and sexual function

- Female participants who have reliable and consistent computer and internet access on a
daily basis

Exclusion Criteria:

- Female participants shall not have an active sexually transmitted disease and/or
infection

- Female participants who are actively undergoing chemotherapy or radiation

- Female participants who are currently taking any cancer-related or photosensitivity
drugs

- Female participants who are pregnant, who may think they are pregnant, and/or actively
trying to get pregnant during the clinical study