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MassDevice
11 小时
EndoQuest wins FDA IDE to study surgical robot in colorectal surgery
EndoQuest Robotics announced today that it received FDA investigational device exemption (IDE) for a study of its surgical ...
MassDevice
13 小时
Pentax wins FDA nod for new models of endoscopes
Pentax Medical announced today that it earned FDA 510(k) clearance for new models of its i20c video endoscope series.
MassDevice
13 小时
The top medtech stories of 2024
AFib-treating cardiac ablation, surgical robotics, nitinol and diabetes treatment tech lead among this year’s top medtech ...
MassDevice
14 小时
Siemens Healthineers acquires Novartis molecular imaging business
Siemens Healthineers announced today that it completed the acquisition of Advanced Accelerator Applications Molecular Imaging ...
MassDevice
14 小时
FDA grants humanitarian device exemption to Artivion’s aortic arch remodeling device
Artivion (NYSE:AORT) this week announced it received FDA humanitarian device exemption (HDE) for its AMDS Hybrid Prosthesis.
MassDevice
15 小时
Terumo, Medis announce strategic partnership to enhance cardiovascular care
Terumo Health Outcomes and Medis Medical Imaging today announced a strategic partnership to enhance cardiovascular care in ...
MassDevice
16 小时
Second Heart Assist concludes mechanical circulatory support trial
Second Heart Assist announced today that it completed the third in a planned series of studies for its mechanical circulatory ...
MassDevice
16 小时
Microbot Medical submits Liberty surgical robot to FDA
Microbot Medical (Nasdaq:MBOT) announced today that it submitted an FDA 510(k) premarket notification for its Liberty ...
MassDevice
1 天
AngioDynamics wins FDA clearance for NanoKnife system in prostate tissue ablation
AngioDynamics received FDA 510(k) clearance for its NanoKnife system for prostate tissue ablation in intermediate-risk ...
MassDevice
1 天
Medtech M&A could be on the rise in 2025
Analysts from Bank of America predict a favorable environment for mergers and acquisitions in the medtech space in 2025.
MassDevice
1 天
SetPoint Medical submits neuromod device to FDA
SetPoint Medical announced today that it filed with the FDA for premarket approval (PMA) of its neuroimmune modulation device ...
MassDevice
1 天
InspireMD begins pivotal study of CGuard Prime in TCAR procedures
InspireMD enrolled the first patient in its CGUARDIANS II pivotal study, which will evaluate the CGuard Prime Carotid Stent ...
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