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# Electrical Stimulation Device for Premature Ejaculation
- URL: https://www.fdaweb.com/electrical-stimulation-device-for-premature-ejaculation/
- Published: 2022-06-03T12:00:00.000Z
- Updated: 2026-09-14T17:47:21.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5151969

*Federal Register* notice: FDA is classifying the non-implanted electrical stimulation device for management of premature ejaculation into Class 2 (special controls). The action was based on a Virility Medical request for de novo classification of its vPatch. The agency has identified it as a device intended to be used in patients with premature ejaculation by delivery of electrical stimulation to the perineal muscles and nerves. To view the notice, click [here](https://public-inspection.federalregister.gov/2022-12082.pdf?ref=fdaweb.com).