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Aesthetic Medicine
FDA clears VelaSmooth for cellulite treatment
July 12th, 2005
Syneron Medical, Ltd., (ELOS) announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) premarketing clearance to Syneron's VelaSmooth medical device, powered by elos, for the temporary reduction in the appearance of cellulite. The VelaSmooth also received clearance for the relief of minor muscle aches, pain and spasm, and the temporary improvement of local blood circulation. The clearance of the VelaSmooth offers a new nonsurgical, no downtime alternative for patients wishing to treat the appearance of cellulite, according to the company. "The VelaSmooth incorporates a combination of technologies enabling deeper heating and...
Source: Science Letter (2005-07-12)
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