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The dual-use device provides low-dose, high quality images with premium flat detector technology, eliminating the need for several frames to produce a useable image for diagnosis. Read More
In the trial, the company will explore the bone graft’s use as it compares to autografts in transforaminal lumbar interbody fusion procedures meant for treating degenerative disk disease. Read More
The agency determined that the risks posed by the OTC products were well established and premarket notification was not necessary to provide reasonable assurance of the product’s safety and effectiveness. Read More
The product is created with regenerated oxidized cellulose and designed to control bleeding and absorb exudate and drainage from superficial wounds. Read More
The company was awarded a grant of $1.4 million last December for clinical validation of the device by the European Fund for Regional Development. Read More