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BioWorld - Tuesday, January 13, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Dec. 16, 2021

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Fist Assist earns FDA breakthrough device designation for wearable vein dilation device

Fist Assist Devices LLC received a breakthrough device designation from the FDA for its Fist Assist Model FA-1 device for patients with end-stage renal disease (ESRD). The pre-surgical dilation device promotes arteriovenous (AV) fistula creation in renal failure patients with inadequate vein size for creation of an AV fistula for hemodialysis. An AV fistula is a surgical connection between an artery and a vein used as an access point for dialysis. Read More
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FDA’s pressure on 510(k) process a factor in lawsuit between J&J, Auris

The FDA’s regulation of medical technology may be assumed to have a number of unintended consequences, and one of those seems to be the lawsuit between Johnson & Johnson (J&J) and Auris Health Inc. Due to a 2018 FDA policy change regarding 510(k) devices, a robotic surgery system acquired by a J&J subsidiary from Auris was forced into the lengthier de novo premarket channel. This change ultimately helped derail the development effort for the Auris Iplatform surgical system and thus played a role in the $2.35 billion lawsuit alleging that J&J had engaged in fraud in its deal with Auris over the acquisition. Read More
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Investors back multiomics analyzer with $35.4M financing

Depixus Ltd. has raised $35.4 million in an oversubscribed series A financing to push commercialization of its Magna multiomics system. The series A round was co-led by Lansdowne Partners and PSIM Fund, with participation from Casdin Capital and existing investor Arix Bioscience. The funds bring the company's total equity and grant funding to more than $47 million. Read More
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Top Med-tech Trends of 2021: Move over Chevy, smartwatches take the heartbeat of America now

This year saw continued advances in smartwatches as they increasingly move from wellness assistants to medical monitors. Nowhere has that been clearer than in cardiovascular health, where multiple wearables now allow users to quickly detect atrial fibrillation, a notoriously shy condition previously only detectable in early stages by chance in a physician’s office or by wearing a cumbersome Holter monitor for 24 to 48 hours. Read More
Virgile Barret-Vivin and Alexis Saintamand with endoscopy tech

Dyameo raises $1.13M to bring endoscopy probe for in vivo cancer diagnosis to market

PARIS – Dyameo SAS has successfully raised $1.13 million in seed funding to develop its endoscopy probe used for the instantaneous detection of cancerous cells. This round was led by  Medevice SAS and Aquiti Gestion SAS via its co-investment fund, NACO. Read More

Appointments and advancements for Dec. 16, 2021

New hires and promotions in the med-tech industry, including: Bio-Rad, Camber Spine, Davita, Medtronic, Prophase Labs. Read More

Financings for Dec. 16, 2021

Med-tech firms raising money in public or private financings, including: Brainomix, Evotec, Fineheart, Perimeter Medical Imaging AI, Sunrise, Tasso. Read More

In the clinic for Dec. 16, 2021

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Ultromics. Read More

Other news to note for Dec. 16, 2021

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biocorp, Boyd, Caredx, Cerba, Heitkamp & Thurman, H&T Presspart, Hyperfine, Itamar Medical, Kardium, Know Labs, Life Tech Scientific, MBK Tape, Medtronic, Olympus, Onward, Viroclinics-DDL, Zoll. Read More

Regulatory actions for Dec. 16, 2021

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Applied Biocode, Fist Assist, Mdoloris, Mindray. Read More

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