Hologic Inc. announced that the U.S. Food and Drug Administration (FDA) approved the use of Hologic's new C-View 2-D imaging software. C-View 2-D images may now be used in place of the conventional 2-D exposure previously required as part of a Hologic 3-D breast tomosynthesis screening exam.

Philips Healthcare announced that CX50 xMatrix, the first portable ultrasound with Philips' Live 3-D transesophageal echo (TEE), now offers 2-D intracardiac echo (ICE) capability. The CX50 xMatrix with available Live 3-D TEE and ICE was first shown in Paris at the EuroPCR in May.

The Canvys Healthcare team has launched its new Image Systems 6MP (megapixel) display with LED backlights, and the quality control (QC) Vue browser-based, zero-footprint QC tool for mobile devices and displays. The new 30-inch widescreen, color display features LED backlights that provide high brightness and contrast.

Sensus Healthcare has received clearance from the U.S. Food and Drug Administration (FDA) to treat Keloids with the SRT-100. The SRT-100 is an alternative to surgery in treating non-melanoma skin cancer and now is approved to treat keloids caused by surgery or injury. Leading dermatologists and oncologists have found the SRT-100 superficial radiotherapy system to be a choice for their patients who are not good surgical candidates. Sensus Healthcare has reintroduced superficial radiotherapy (SRT) to the global clinical community as a viable, safe, and cost-effective modality to treat non-melanoma skin cancers and keloids in hospitals and private practice settings.