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FUJIFILM Healthcare Americas Corporation recently announced that 510k clearance has been obtained for the new EG-740UT1 linear endoscopic ultrasound (EUS) scope, which is compatible with the Fujifilm ARIETTA 8502 ultrasound processor. The ARIETTA 850 is the...
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Johnson & Johnson MedTech* has announced that DePuy Synthes, The Orthopaedics Company of Johnson & Johnson**, has secured 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its TELIGEN System, an integrated technology platform that...
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joimax is launching a new endoscopic surgical system, TESSYS® TransSAP. joimax is releasing the TESSYS TransSAP – the fourth addition to the TESSYS family encompassing the standard TESSYS Std, TESSYS XT featuring longer reach instruments, and TESSYS Thx, the optimized...
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An analysis of race-related patient safety reports by ECRI, the nation’s largest nonprofit patient safety organization, shows that both patients and healthcare providers are frequently on the receiving end of inappropriate comments about race. A review of more than...
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The United States Food and Drug Administration (FDA) has granted 510(k) clearance to Abiomed (Nasdaq: ABMD) for its Impella Low Profile Sheath. Compared to the existing 14 French (Fr) sheath used for placement of Impella CP, the new sheath maintains the same inner...
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LiveData, a data-driven surgical care company, has announced the integration of PREFcards, a cloud-based, surgical preference card system, to add operational efficiency and accuracy to surgical workflows. Combining LiveData’s field-proven PeriOp Manager with...
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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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