Close

Search

Search Menu
Photonics Media Photonics Buyers' Guide Photonics EDU Photonics Spectra BioPhotonics EuroPhotonics Industrial Photonics Photonics Showcase Photonics ProdSpec Photonics Handbook
More News
share
Email Facebook Twitter Google+ LinkedIn Comments

Candela Wind FDA Ok for Skin Laser

BioPhotonics
Nov 2007
The FDA has approved the Serenity device from Candela Corp. of Wayland, Mass., for use during all laser and intense pulse light treatments. The device uses vacuum-driven pneumatic skin-flattening technology originally developed by Inolase Ltd. of Netanya, Israel, to compress the skin during treatment, thereby blocking the transmission of pain signals. The device previously had been approved for use in hair removal treatments.

Biophotonicshair removal treatmentsintense pulse light treatmentsNews & Featureslasers

Comments
Terms & Conditions Privacy Policy About Us Contact Us
back to top
Facebook Twitter Instagram LinkedIn YouTube RSS
©2018 Photonics Media, 100 West St., Pittsfield, MA, 01201 USA, info@photonics.com

Photonics Media, Laurin Publishing
x Subscribe to BioPhotonics magazine - FREE!
We use cookies to improve user experience and analyze our website traffic as stated in our Privacy Policy. By using this website, you agree to the use of cookies unless you have disabled them.