OR Today Magazine

Catalyst OrthoScience Inc. has announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its Archer Patient-Specific Instrumentation (PSI).

Cara Medical Ltd. recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the CARA System, a computed tomography angiography (CTA)-based platform that provides noninvasive, patient-specific three-dimensional (3D) visualization of the cardiac conduction system.

The U.S. Food and Drug Administration (FDA) has cleared the new Xenocor Saberscope, a single-use 5mm articulating laparoscope designed for high-definition (HD) visualization during minimally invasive abdominal (belly) and thoracic (chest) surgical procedures.

Olympus Corp. of the Americas has announced FDA clearance of the pediatric use indication for two single-use bronchoscopes in the respiratory portfolio distributed by Olympus.

The Accreditation Association for Ambulatory Health Care (AAAHC) will host its flagship Achieving Accreditation educational program March 19-20, 2026, at the Renaissance Orlando at SeaWorld in Orlando, Florida.