EndyMed Medical has announced it has received FDA clearance for its GLOW device, according to a news release.
The device, along with two treatment handpieces, was approved for use for dermatologic procedures to help reduce mild to moderate facial wrinkles and fractional RF skin resurfacing.
"The GLOW by EndyMed and our 3DEEP technology is already in use by a large number of customers throughout Europe and Asia, and we are very excited to be able to offer it to the U.S. market," said EndyMed CEO Uzi Blumensohn, in the release. "We receive reports about amazing treatment results and high customer satisfaction levels, and we firmly believe that the GLOW by EndyMed will be a success in the United States as it is in the rest of the world."
The GLOW will be available in the United States through Eclipse Aesthetics.
EndyMed Medical is headquartered in Caesarea, Israel.
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