Candela Receives FDA Clearance for Its Serenity(TM) Device for Additional Aesthetic Laser Applications (Business Wire via Yahoo! Finance)
WAYLAND, Mass.----Candela Corporation today announced that it received an additional FDA clearance for the Serenity device using Pneumatic Skin Flattening (PSF) technology. This clearance enables the use of the Serenity device for the reduction of pain during all laser and intense pulse light treatments.

FDA Accepts for Review Complete Response to Approvable Letter for Entereg(R) (alvimopan) for POI (Business Wire via Yahoo! Finance)
EXTON, Pa. & PHILADELPHIA----Adolor Corporation and GlaxoSmithKline announced today that the U. S. Food and Drug Administration has accepted as complete, Adolor's response to the November 2006 New Drug Application approvable letter for Entereg for the management of postoperative ileus .