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The company’s LockeT suture retention device has demonstrated immediate hemostasis and short times to ambulation in clinical studies. The VIVO™ non-invasive mapping system has been highlighted in peer-reviewed publications as a meaningful tool for guiding ablation therapy. Ongoing multicenter studies are evaluating both products’ effectiveness and workflow improvements. Over 130 patients have been enrolled in the comparative LockeT II study; European registry data on VIVO™ will be published through 2025.[7]
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