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Unit developed with Cynosure expected out in 2013.
July 19, 2012
By: TOM BRANNA
Editor
Cynosure, Inc. has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market a home-use over the counter device for the treatment of facial wrinkles. The device, which was developed in partnership with Unilever, is expected to be launched commercially by in 2013. “FDA clearance of this device marks a significant milestone in our alliance with Unilever to develop light-based devices for the consumer market,” said Michael Davin, Cynosure’s presiden...
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