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# Viveve Gains Clearance to Increase Manufacturing
- URL: https://www.fdaweb.com/viveve-gains-clearance-to-increase-manufacturing/
- Published: 2020-12-03T12:00:00.000Z
- Updated: 2026-09-14T16:38:51.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148225

FDA has cleared a Viveve Medical 510(k) to expand its manufacturing capacity for its consumable treatment tips used with the company’s Cryogen-cooled Monopolar Radiofrequency (CMRF) technology. CMRF is used with the Viveve System, which is indicated for use in general surgical procedures for electrocoagulation and hemostasis. Viveve says it has also begun clinical development programs for the device’s use in treating stress urinary incontinence and sexual dysfunction.