Jay Reyero Discusses in AmSpa Podcast FDA Warning on Vaginal Rejuvenation Devices

Samuel E. Pondrom | 8.8.18


In its Medical Spa Insider Podcast series, the American Medical Spa Association talked with Jay Reyero regarding the recently issued warning by the Food and Drug Administration (“FDA”) concerning medical devices used for vaginal rejuvenation.

On July 30, 2018, the FDA issued a warning to alert patients and health care providers that the use of energy-based devices to perform vaginal rejuvenation may be associated with serious adverse events and there are currently no devices approved by the FDA for such use.

In the podcast, Jay talks with AmSpa about “off-label use” and the practical implications of the FDA warning for health care providers and medical spas currently performing the procedure.

Listen to Jay on Episode 12: What Does the FDA Alert Regarding Feminine Rejuvenation Mean for Medical Spas?