TGA Approves Osteopore’s 3D-Printed Scaffolds for Bone Regeneration April 21, 2020 The 3-D printed scaffolds dissolve over time to leave only healthy bone tissue. Read More
Astura Gets 510(k) Clearance for Lumbar Interbody Fusion System April 21, 2020 The Sirion system is the company’s first product that combines interbody and fixation options in a single device. Read More
Endospan’s Aortic Arch-Repair System Gets Breakthrough Designation April 21, 2020 The system allows physicians to repair the aortic arch from the inside. Read More
Nova Biomedical Launches Emergency Blood-Testing System April 20, 2020 The lightweight case fits in a medical bag. Read More
Roche Prepares to Launch COVID-19 Antibody Test April 20, 2020 Roche said it plans to obtain CE mark certification in early May and will seek FDA Emergency Use Authorization as well. Read More
Proteomics International Earns CE Mark for Kidney Disease Test April 17, 2020 The test is the first available in the EU for predicting the onset of diabetic kidney disease. Read More
Elekta Earns CE Mark for Radiation-Image Storage System April 16, 2020 The system does not need additional hardware. Read More
Behold.ai Gets CE Mark for Chest X-Ray Diagnosis Tech April 16, 2020 Chest x-rays are the main diagnostic tests for triage of COVID-19 patients. Read More
PathoFinder’s COVID-19 Test Gets CE Mark April 16, 2020 The company expects to deliver thousands of tests in the coming weeks. Read More
Arch Therapeutics’ Topical Gel Gets CE Mark April 15, 2020 The product can be used for complicated and chronic wounds. Read More
Becton Dickinson Earns Clearance for Another COVID-19 Test April 15, 2020 The test can produce results in two to three hours. Read More
FDA Grants Emergency Use of Rutgers’ COVID-19 Saliva Test April 15, 2020 The saliva-based test allows healthcare professionals to avoid the risk of infection from nasopharyngeal and oropharyngeal samples. Read More