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BioWorld - Monday, March 16, 2026
Home » Topics » Medical technology, BioWorld

Medical technology, BioWorld
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Automata LINQ bench lab

Automata secures $45M in series C raise

Jan. 30, 2026
Automata Technologies Ltd. raised $45 million in a series C funding round that included a strategic investment partnership with Danaher Corp. The funds will be used to support the scaling of customer deployments, the building of the next generation of Automata’s data and closed-loop experimentation software platform and the expansion of its global operations.
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Medicare puzzle

CMS rewrites organ procurement rule to expand availability

Jan. 30, 2026
By Mark McCarty
A new draft guidance for organ procurement organizations doing business in the U.S. would seem to tackle some pressing issues with organ donation, such as the conditions in which a problem qualifies as an adverse event. Perhaps of greater interest to companies in the organ container business is that the Centers for Medicare & Medicaid Services is intent on increasing the availability of organ donations to deal with an insatiable demand for donated organs.
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Invest compass
Med-tech financings Q4 2025

Q4 financing boom lifts med-tech to strong 2025 finish

Jan. 30, 2026
By Amanda Lanier
Total med-tech financing activity surged in the fourth quarter of 2025, with $16.21 billion raised across all financing categories, more than double the $5.78 billion recorded in Q3 and the strongest quarterly total of the year.
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4DMedical Respiratory Imaging

4dmedical raises $105M to bolster U.S. CT:VQ lead

Jan. 29, 2026
By Tamra Sami
Australian respiratory imaging technology company 4dmedical Ltd. raised AU$150 million (US$105 million) in an institutional placement to accelerate U.S. adoption of its CT:VQ lung imaging software to bolster the company’s lead in software-based lung imaging.
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3-30-fractyl-revita.png

Fractyl’s Revita reduces post-GLP-1 weight regain 70%

Jan. 29, 2026
By Annette Boyle
Six-month results from the REMAIN-1 trial showed that Fractyl Health Inc.’s Revita procedure cut post-GLP-1 weight regain by about 70% compared with a sham procedure in patients who discontinued incretin-based drugs such as semaglutide and tirzepatide after achieving substantial weight loss.
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En Carta EC Pocket Lyme test

En Carta Lyme disease test wins FDA breakthrough designation

Jan. 29, 2026
By Shani Alexander
En Carta Diagnostics SA's EC Pocket Lyme received FDA breakthrough device designation for its rapid, molecular diagnostic test for the early detection of Borrelia bacteria, which causes Lyme disease. The designation marks a pivotal step for the French startup as it will enable closer interaction with the agency, accelerating its route to market, and getting it to patients sooner.
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Gloved hand holding test tube marked for ataxia-telangiectasia genetic test

Part B Medicare genetic testing spiked in 2024

Jan. 29, 2026
By Mark McCarty
A Jan. 28 report on Medicare spending on lab tests indicated that spending on many types of tests flattened between 2022 and 2024, but spending on genetic tests rose 20% between 2023 and 2024 to $3.6 billion. While the report does not specifically call out fraud as a driver of spending, the U.S. Department of Justice posted a Jan. 26 press release identifying a case of Medicare gene testing fraud that amounted to $52 million, just one of several recent examples of this kind of fraud.
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Gavel and scales

Drug, device makers could still be liable for terrorist attacks

Jan. 26, 2026
By Mari Serebrov
No Comments
In a lawsuit that’s been bouncing through the courts for years, the U.S. Court of Appeals for the District of Columbia once again cleared the way for several biopharma and medical device companies to potentially be held liable, under the Anti-Terrorism Act, for terrorist attacks against hundreds of Americans in Iraq.
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Decorative scales of justice in a courtroom

FY 2025 a banner year for US False Claims Act recoveries

Jan. 20, 2026
By Mark McCarty
The U.S. Department of Justice said recoveries under the False Claims Act in fiscal year 2025 reached a record of more than $6.8 billion, more than 80% of which came from health care cases.
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PET imaging

Radiopharm Theranostics’ RAD-101 meets brain metastases endpoints

Dec. 16, 2025
By Tamra Sami
Radiopharm Theranostics Ltd.’s radiotracer RAD-101 met the primary endpoint in 92% of patients in the phase IIb imaging trial in brain metastases, according to interim results. To date, 11 of the 12 patients treated with RAD-101 (F18-Pivalate) achieved concordance with MRI (the primary endpoint) as assessed by PET imaging of brain metastases. The results showed significant and selective tumor uptake, and images confirm metabolic activity in brain metastases compared to equivocal MRI findings.
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