Home » Bioengineered skin wins approval from the FDA. Bioengineered skin wins approval from the FDA July 1, Reprints Share. Opinions vary on the bioethics of bioengineered skin. New skin growth: From test tube to body. Bioengineered skin wins approval from the FDA Apligraf approved for venous skin ulcers The federal Food and Drug Administration has given approval for the use of the human skin equivalent Apligraf in the United States.
Report Abusive Comment Thank you for helping us to improve our forums. Is this comment offensive? Please tell us why. Restricted Content You must have JavaScript enabled to enjoy a limited number of articles over the next days. Please click here to continue without javascript.. Wound Care It contains living cells, proteins produced by the cells, and collagen. Complications may include suspected wound or non-wound infection, skin inflammation, wound drainage, swelling, a skin tear or cut, pain, a new ulcer, red, flaky skin, bone infection, rash, low or high blood sugar, bruising, swelling, worsening ulcer, and dry skin.
Apligraf should not be used if your wound is infected or if you are allergic to cow collagen or the agarose shipping medium. For more information, please read the complete prescribing information available at Apligraf.
Having pioneered the field, Massachusetts-based Organogenesis Inc. The company's mission is to bring the medical marvel of regenerative medicine products to patients and to standardize their use in everyday medical care. For more information, visit www. About Organogenesis Inc.
Economic outcomes among Medicare patients receiving bioengineered cellular technologies for treatment of diabetic foot ulcers. J Med Econ. Hospitalizations due to diabetic foot in Switzerland.
Rev Med Suisse.
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