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Every perioperative nurse has asked the question: “Is there a better way to do this?” Maybe it’s about preventing surgical site infections, improving team communication during handoffs or helping patients recover faster. These everyday questions are the seeds of research, but they need something critical to grow – funding.
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Catalyst OrthoScience Inc. has announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its Archer Patient-Specific Instrumentation (PSI).
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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.
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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.
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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.
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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.
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For over 20 years, OR Today has provided perioperative and SPD professionals with up-to-date news and information about their profession. The magazine aims to educate readers about new guidelines, techniques, and equipment, as well as practical information for career building, problem-solving and overall well-being.
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