The energy based devices for vaginal “rejuvenation,” urinary incontinence, vaginal cosmetic procedures, and other vulvo‐vaginal disorders: An international multidisciplinary expert panel opinion

Author:

Digesu Giuseppe Alessandro1ORCID,Tailor Visha1,Preti Mario2,Vieira‐Baptista Pedro34,Tarcan Tufan5,Stockdale Colleen6,Mourad Sherif7

Affiliation:

1. Imperial College HealthcareDepartment of UrogynaecologyLondonUK

2. Department of Obstetrics and GynecologyUniversity of TorinoTorinoItaly

3. Hospital Lusíadas PortoPortoPortugal

4. Lower Genital Tract UnitCentro Hospitalar de São JoãoPortoPortugal

5. Marmara University School of MedicineDepartment of UrologyIstanbulTurkey

6. Department of Obstetrics and GynecologyUniversity of IowaIowa CityIowa

7. Ain Shams UniversityDepartment of UrologyCairoEgypt

Publisher

Wiley

Subject

Urology,Neurology (clinical)

Reference29 articles.

1. U.S. Food and Drug Administration. 510(k) Summary for RevLite Q‐Switched Nd:YAG Laser System [letter]. Silver Spring (MD): FDA; 2014. Available at:http://www.accessdata.fda.gov/cdrh_docs/pdf13/k133254.pdf. Retrieved May 19 2016.

2. ACOG Committee Opinion No. 378: Vaginal “Rejuvenation” and Cosmetic Vaginal Procedures

3. FDA Warns Against Use of Energy‐Based Devices to Perform Vaginal “Rejuvenation” or Vaginal Cosmetic Procedures: FDA Safety Communication.https://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm615013.htm.

4. Vulvar and vaginal fractional CO2 laser treatments for genitourinary syndrome of menopause

5. U.S. Food and Drug Administration. Re: trade/device name: DEKA SmartXide2 Laser System [letter]. Silver Spring (MD): FDA; 2014. Available at:http://www.accessdata.fda.gov/cdrh_docs/pdf13/k133895.pdf. Retrieved May 19 2016.

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