FDA approves Viberect device for treatment of erectile dysfunction


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Chambersburg, Pennsylvania-based medical device technology developer Reflexonic has received FDA approval for its Viberect device aimed at men with mild to moderate erectile dysfunction (ED) symptoms, including those undergoing post-prostatectomy erectile rehabilitation and those with spinal cord injuries causing ejaculatory dysfunction. Instead of relying on a little blue pill to get things ready for the bedroom, the device, which looks a bit like a hair crimper, delivers targeted nerve stimulation to both dorsal and ventral surfaces of the penis using medical Softpads.


In addition to helping strengthen and maintaining the rigidity of an erection, Reflexonic also says, "subsequent orgasm and ejaculation is greatly amplified."


Quoting a recent epidemiological study of the use of vibrators by American women and men, Reflexonic says vibratory stimulation, like that delivered by the Viberect, is considered safe by the medical community. The company says the device has been demonstrated to be a safe and effective device for provoking erections for men who suffer from mild to moderate ED and men who have suffered spinal cord injuries.


Reflexonic obtained final FDA approval for Viberect to be sold with a doctor's prescription in June and plans to begin sales of the device this northern summer at a price yet to be announced. Sales will be through the Reflexonic website and it will ship orders worldwide.

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