FDA alerts users to issue with Olympus’s endoscope component after patient death
The US Food and Drug Administration (FDA) has issued an alert relating to a problem with a component on endoscopes …
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Castle Biosciences reports preliminary data from atopic dermatitis test study
Castle Biosciences has reported preliminary data from its ongoing study of an atopic dermatitis (AD) pipeline test for individuals with …
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FDA approves mini version of RECELL GO for smaller wounds
The US Food and Drug Administration (FDA) has approved a premarket approval (PMA) supplement for Avita Medical’s RECELL GO mini, …
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EVLP platform enables transplants of marginal lungs in UK hospitals
The first successful double-lung transplant using Xvivo's XPS system has taken place in the UK. XPS is an ex-vivo lung perfusion …
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Signati submits De Novo application to FDA after completing trial
Signati Medical has completed a trial evaluating its device that aims to streamline vasectomy procedures, and submitted a De Novo …
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Investors optimistic about continued biotech and medtech IPO resurgence in 2025
When Australian biotech Telix Pharmaceuticals pulled a last-minute plug on its US public listing, it was yet another sign that …
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Sequana shares surge after FDA approval for alfapump
The US Food and Drug Administration (FDA) has approved Sequana Medical’s alfapump for the treatment of recurrent or refractory ascites …
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Merit Medical’s WRAPSODY device gains FDA premarket approval
Merit Medical Systems has received premarket approval from the US Food and Drug Administration (FDA) for its WRAPSODY Cell-Impermeable Endoprosthesis …
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Medical Device Network Excellence Awards 2024: Novius
Novius, a pioneering Japanese startup specializing in medical imaging technology, has been recognized with the Innovation Award in the 2024 …
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The 10 biggest medtech stories of 2024
As another year draws to a close, we look at the most consequential stories and emergent themes of the year …
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Sotelix raises $1.7m to advance therapeutic endoscopy development
Sotelix Endoscopy has completed a $1.7m funding round that will go towards research, development and the in vivo testing of …
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Onward wins FDA approval for ARC-EX system in spinal cord injury patients
The US Food and Drug Administration (FDA) has granted de novo classification to Onward Medical for its ARC-EX system in …
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Mainz Biomed partners with Quest for colorectal cancer screening test
Mainz Biomed has announced a partnership with Quest Diagnostics to support the commercialisation of its NextGen colorectal cancer screening test, …
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What’s ahead for Nvidia in life sciences in 2025
2024 has been a good year for US-based technology powerhouse Nvidia. The company has come a long way from their …
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Health tech company ŌURA secures $200m in Series D funding
Finnish health technology company ŌURA has secured $200m in a Series D funding round, raising the company’s valuation to $5.2bn. Fidelity …
