Page 29 - Breakthrough Device News Today

/PRNewswire/ -- Diadem srl, a company developing blood-based tests for the early prediction and diagnosis of Alzheimers disease (AD), today announced that it...

Medtech companies are increasingly looking to the FDA instead of Europe's CE mark when launching novel products, according to a new report.

Surgical Sutures Market Share Analysis, By Product Type (Absorbable Surgical Sutures, Non-Absorbable Surgical Sutures), By Raw Material (Polyglycolic Acid...

/PRNewswire/ -- 3Spine, Inc., a U.S. medical device company developing total joint replacement for the lumbar spine, has raised $33 million in an...

/PRNewswire/ -- 3Spine, Inc., a U.S. medical device company developing total joint replacement for the lumbar spine, has raised $33 million in an...

Press release content from PR Newswire. The AP news staff was not involved in its creation.

Recent progress includes feasibility study completion and nearly 2,000 patient treatments

According to Fact MR’s recent market research, sales of Absorbable Surgical Suture to swell at propelled CAGR through 2031, as investment towards expansion of healthcare infrastructure continues rising. The goal of the survey is uncover growth opportunities, key trends, growth drivers, and challenges. It also provid...

The FDA 510k-cleared Fist Assist FA-1 wearable device received Breakthrough Device designation late last year and the device maker is looking to raise capital through equity crowdfunding in May. Outside the U.S., it is approved for increased arm vein dilation and AV fistula dilation/maturation.

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