Hologic, Inc. 通过乳腺健康产品组合的广度保持竞争地位,该组合符合成像、活检工作流程需求,以及从筛查到诊断路径的程序效率期望。产品策略通常强调系统的可用性、一致的样本采集以及与影像引导程序的兼容性,以支持高容量的临床环境。商业吸引力得益于医院和诊断网络的采用模式,这些模式优先考虑简化的工作流程和可预测的性能。随着同行扩展模态覆盖并改进设备的人体工学和消耗品选项,乳腺癌核心针活检市场竞争依然活跃。
2026年1月,BD(Becton, Dickinson and Company)获得FDA 510(k)认证,用于EnCor EnCompass乳腺活检和组织移除系统,这是一种新的多模式乳腺活检平台,旨在允许临床医生使用单一集成系统在各种成像模式下执行微创乳腺活检,计划于2026年初商业推出。
2026年3月,Mammotome(Danaher公司)获得FDA认证,用于Mammotome Prima MR双真空辅助乳腺活检系统,这是首个MR引导的乳腺活检解决方案,设计用于放置在MRI扫描仪室内患者旁边,以及HydroMARK Plus乳腺活检标记器,提升MR引导乳腺活检程序中与核心针活检应用相关的精确度和工作流程。
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Thank you for the data! The numbers are exactly what we asked for and what we need to build our business case.
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The report was an excellent overview of the Industrial Burners market. This report does a great job of breaking everything down into manageable chunks.