Apyx Medical Corporation, a maker of medical devices and supplies and the developer of Helium Plasma Technology, marketed and sold as Renuvion and J-Plasma in surgical markets, announced it has received 510(k) clearance from the FDA for the use of the Renuvion Dermal Handpiece for specific dermal resurfacing procedures.
The FDA has approved the Magnetom Spectra 3 Tesla MRI system, from Siemens. The new system employs Tim (Total imaging...
Philips launches Ingenia Ambition X 1.5T MR with industry-first fully sealed magnet for more productive, helium-free operations. Royal Philips has...