Aug 7, 2018 · Medical device manufacturers are deceptively marketing energy-based therapies for vaginal rejuvenation—an unapproved, risky procedure that ...
We track FDA activity to give you the latest updates on recalls, meetings, hearings and safety investigations. Top Articles on FDA Regulation.
Jul 30, 2018 · FDA warns doctors and patients about deceptive claims on laser medical devices used to treat menopausal symptoms for “vaginal rejuvenation”
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The Food and Drug Administration (FDA) has reclassified the vaginal mesh medical device to reflect a higher risk of adverse side effects after thousands of ...
A photo depicting a doctor talking with diabetes patient after FDA warns of rare genital gangrene. FDA Regulation. FDA Warns of Rare Genital Gangrene Linked to ...
Mar 12, 2019 · Advocates for BIA-ALCL awareness call on women and medical professionals to get serious about textured breast implant risks. The FDA will ...
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Aug 27, 2018 · She'll discuss gender bias in health treatment, failures of federal device regulation ... FDA announcement of vaginal rejuvenation treatment Photo ...
Feb 22, 2022 · The use of lasers for so-called vaginal rejuvenation is not only ineffective but dangerous. The FDA needs to reclassify these devices.
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... Articles for. Medical ... FDA Approves OTC Hearing Aid Rules. MedTruth ... FDA Regulation · Doctor charged in transvaginal mesh surgery scheme consulting with ...
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Follow our in-depth articles to explore the odd and ends of health care, tips for improving your health, underreported medical conditions and more. Wellness ...
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