Fda approved facial regenerator

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Portrait® PSR3 (Rhytec, Inc.) has been approved by the U.S. Federal Drug Administration (FDA) for the treatment of facial rhytides, superficial skin lesions, and. Portrait® PSR device is the first non-laser technology approved by the FDA and which contributes to the formation of facial lines, sagging skin and wrinkles.
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Plasma skin regeneration is a new technology that uses plasma energy to regenerate the skin. Federal Drug Administration FDA for the treatment of facial rhytides, superficial skin lesions, and actinic keratoses for full face and regional resurfacing eyes and mouth. FDA approval for the chest, neck, hands, and acne scarring has been requested but not yet granted. We are evaluating this technology, which uses nitrogen plasma discharge as its energy source rather than light or radio frequency emission. Although there are no published outcomes studies yet, our initial results have been promising. In our series of close to 20 sites, mainly periorbital and periorofacial, there is evidence of good collagen remodelling and diminished rhytids and patient satisfaction.
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    Plasma skin regeneration PSR , is a non-laser treatment that uses a device to deliver energy in the form of plasma to rejuvenate skin by improving facial lines and wrinkles rhytides and skin pigmentation associated with photoaging.

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