Start-Up News September 2006

Ample Medical finds ample room for improvement in heart valve repair; glucose monitoring attracts Glucon, GlucoLight and VivoMedical.

In June, Medtech Insight and Windhover Information’s In3 Medical Device Summit in San Francisco—the largest investment and partnering meeting in the medical device industry—showcased some 80 young medical device companies in high-growth segments of the industry across all major clinical segments. Companies unveiled strategies to crack such emerging markets as percutaneous heart valves, noninvasive glucose monitoring, minimally invasive spine, obesity management, cardiovascular imaging, and convergence opportunities for devices and biotherapeutics, to name only a few of the device markets highlighted. Some of these presenters and their technologies are highlighted below.

Mitral regurgitation (MR) is a common consequence of congestive heart failure, and one that contributes to the vicious circle of...

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Patients With Movement Disorders Will Benefit From Medtronic’s Expanded MRI Labeling For DBS

 
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Medtronic announced it received expanded MRI labeling for its DBS systems, which is critical, given that almost 70% of all DBS-eligible patients will likely need an MRI at some point in their care, says Ashwini Sharan, CMO for Medtronic Neuromodulation.

Podcast: Lung Life AI CEO Shares Regulatory And Reimbursement Journey For Lung Cancer Diagnostic

 

In this episode, Medtech Insight reporter Natasha Barrow speaks to LungLife AI CEO Paul Pagano. Lung Life AI is a US-based AIM-listed medical technology company that has developed a liquid biopsy test for the early detection of lung cancer called Lung LB. Pagano runs through the highlights of Lung Life AI journey to date and its future ambition for a strategic partnership. He also provides advice to similar diagnostic companies seeking reimbursement andcompliance with the US FDA Lab Developed Test ruling.

More from Medtech Insight

Dxcover Launches US Operations With New Headquarters In Tennessee

 

Dxcover sets up new Clinical Laboratory Improvement Amendments (CLIA) lab in Franklin, Tennessee.

EnsoData Boosts AI Sleep Tech With $20M Series B Funding, Targets Underdiagnosis Crisis

 
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EnsoData positions itself as device-agnostic and interoperable, with FDA-cleared software that can integrate with all major devices. CEO Mortara said this flexibility helps maximize patient reach by enabling both direct provider engagement and integration with device manufacturers.

FDA Blocks Some Olympus Endoscopes From Entering US

 

After multiple warning letters and safety communications, the US FDA has decided to block the import of certain endoscopes from Olympus. In total, the agency’s action pertains to 58 device models manufactured by the Japanese firm used in urinary, respiratory, abdominal and pelvic procedures.