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BioWorld - Tuesday, March 24, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Jan. 12, 2024

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Medtronic Percept RC

FDA greenlights Medtronic sensing-enabled DBS system

Medtronic plc received the greenlight from the U.S. FDA for its latest deep brain stimulation system, the Percept RC. The rechargeable neurostimulator includes the company’s sensing technology which captures data from brain signals and allows for more personalized therapy. Read More

First PFA device granted NMPA approval in China

Sichuan Jinjiang Electronic Medical Device Technology Co. Ltd. received approval from China’s National Medical Products Administration (NMPA) approval for the commercial use of its PFA technology in the treatment of atrial fibrillation, making it the first pulsed field ablation device to gain approval in the country. Read More
Patent illustration

USPTO’s new enablement guidelines push for consistency

The U.S. Patent and Trademark Office (USPTO) published new enablement guidelines Jan. 10 to provide more consistency across technologies to ensure patent applications truly enable the breadth of their claims in keeping with the Supreme Court’s unanimous decision last year in Amgen Inc. v. Sanofi SA. Read More

US FDA recognizes hydrogen peroxide as category A sterilant

The ongoing controversy over the use of ethylene oxide (EtO) as a medical device sterilant has yielded a certification by the U.S. FDA for hydrogen peroxide as an alternative category A sterilant. The news is a welcome bit of relief for industry and for patients as the Environmental Protection Agency still seems bent on imposing what some in industry see as draconian controls on EtO, which is still employed to sterilize half of all medical devices used in the U.S. each year. Read More
Illustration of prescription pill bottle with DNA on the label.

Whole genome sequencing improves outcomes in multiple tumor types

A landmark, real-world study in the U.K. has demonstrated that combining whole genome sequencing with clinical data enabled tailored cancer treatment and improved outcomes. At one health care center, having DNA sequence data led to changes from usual standard of care in 25% of cases. “Mostly, [patients] got into clinical trials; some got medicines they wouldn’t have got. Others avoided medicines because their genetic make-up suggested that if they were exposed to the medicines, they would be at risk of harm,” said Mark Caulfield, professor of clinical pharmacology at Queen Mary University of London, who is co-author of a paper outlining the findings in Nature Medicine, Jan 11, 2024. Read More
IRG respiratory disease management system

Immersive Reality details respiratory disease management system

In what represents the first patenting from Immersive Reality Group LLC, the company’s co-founders describe their Intellighealth system for detecting the early onset of respiratory diseases using artificial intelligence and wearable remote health monitoring technologies. Read More

Holiday notice

BioWorld's offices will be closed in observance of Martin Luther King Jr. Day in the U.S. No issue will be published Monday, Jan. 15. Read More

Appointments and advancements for Jan. 12, 2024

New hires and promotions in the med-tech industry, including: Medtronic, Penumbra, Seastar, Symbiosys. Read More

Financings for Jan. 12, 2024

Med-tech firms raising money in public or private financings, including: Rune Labs. Read More

Other news to note for Jan. 12, 2024

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Clinchoice, CSI Medical, Extremity Medical, Henry Schein. Read More

Regulatory actions for Jan. 12, 2024

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Darmiyan, Inkspace Imaging, Neuralace, Pursuant Health. Read More

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