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FDA Warns of Danger of Restoration Equipment

MessagePosté: 19 Juil 2021 7:37
par pippy
Let's understand each other first. Lasers for the vagina are now real. Plus, the Food and Drug Administration (FDA) is already warning you that you should carefully consider it before making a decision. I'm not talking about laser hair removal. But it's a laser "tightening" and "rejuvenating" the vagina, which results in severe burns and horrifying scars.

We know that some medical device manufacturers may advertise their devices with reference to vaginal 'rejuvenation' and/or vaginal plastic surgery. But not to mention the safety and efficiency of the device. Although these devices have been approved by the Food and Drug Administration (FDA) for the treatment of both genital warts and the lining of the cervix with precancerous lesions, these devices are not available. However, its use to "rejuvenate" the vagina has not been approved, which may include tightening a loose vagina or increasing libido. Its use is not currently approved or approved for the treatment of any symptoms or diseases associated with menopause. urinary incontinence or sexual development The Food and Drug Administration (FDA) has also sent a warning letter to the device's manufacturers, MonaLisa Touch and Femilift, to stop promoting vaginal rejuvenation lasers.

Vaginal laser surgery involves cutting the vaginal tissue to stimulate collagen and thicken the vaginal skin. But there can also be increased risks, such as vaginal burns, scarring, and chronic pain. These products are high-risk and there is not enough evidence to support them. The Food and Drug Administration (FDA) is concerned that women are in danger. The American College of Obstetricians does not currently support the use of laser vaginal rejuvenation devices. But it seems that a number of doctors are trying to offer such a service anyway. If your doctor is using or recommending that you use a vaginal tightening or "rejuvenating" device, the FDA warns that you should stop treatment immediately and please report problems to MedWatch, an adverse event reporting program. FDA

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MessagePosté: 19 Juil 2021 9:10
par Clintonagose
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