LED Medical Diagnostics (TSX:LMD) said today its subsidiary LED Dental won FDA 510(k) clearance for its Tuxedo digital intraoral radiography system. The Atlanta, Ga.-based company’s Tuxedo imaging platform consists of an intraoral sensor and image management software, and is designed as a digital replacement for analog dental film. “We’re excited about bringing our own digital intraoral […]
Ex-KCI CEO Burzik dives into venture capital | Personnel Moves
Baxter’s Artiss sealant wins FDA clearance for face-lift procedures | Regulatory Roundup
Baxter International Inc. (NYSE: BAX) won an expanded indication for its Artiss fibrin sealant, making it available for use during in sealing tissue flaps during face-lift surgeries.
Artiss first won FDA clearance in 2008 for use in adhering skin grafts in wound beds prepared for treating burns in adults and children over the age of one.
MassDevice Network
@MassDevice
LinkedIn
YouTube