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BioWorld - Tuesday, May 26, 2026
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Medical technology
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Other news to note for Aug. 10, 2022

Aug. 10, 2022
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biorez, Clarified Precision Medicine, Conmed, Jiqing Biomedical, Metabolon, Sonex, Viecure, Wetrade.
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In the clinic for Aug. 10, 2022

Aug. 10, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Bostongene.
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Financings for Aug. 10, 2022

Aug. 10, 2022
Med-tech firms raising money in public or private financings, including: Atreo, Kurve, Quipt, Sannova.
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Appointments and advancements for Aug. 10, 2022

Aug. 10, 2022
New hires and promotions in the med-tech industry, including: Miromatrix, Nuvasive, Physiq, Qardio, Vitalconnect, Wellthy.
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Consensus statement could boost utilization for intravascular ultrasound

Aug. 9, 2022
By Mark McCarty
Intravascular ultrasound (IVUS) is an established method for gaining an appreciation of the sources of closure of the coronary arteries, but its use in the peripheral vasculature is not quite as well established. Nonetheless a new paper makes the case that IVUS may be appropriate for widespread use in connection with diseases of the peripheral vasculature, a position that could lead to a considerable expansion of sales of IVUS systems.
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Man undergoing MRI scan for prostate cancer diagnosis

FDA advances AI-enhanced tech for prostate diagnosis and treatment

Aug. 9, 2022
By Annette Boyle
Recent U.S. FDA actions could transform decades of prostate cancer care. Two companies focused on prostate cancer received good news from the FDA for their artificial intelligence (AI)-driven software. Bot Image Inc. gained FDA clearance for its medical device computer-aided detection and diagnostic tool, Prostatid. The agency also provided FDA investigational device exemption for Avenda Health Inc.’s Focalpoint ablation system that enables more accurate mapping of a patient’s prostate cancer for better surgical results.
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3D heart illustration showing tricuspid and bicuspid valves

NICE not sold on devices for tricuspid valve repair, annuloplasty

Aug. 9, 2022
By Mark McCarty
The U.K. National Institute for Health and Care Excellence (NICE) issued a pair of health technology assessments related to regurgitation of the tricuspid valve, one each for valve leaflet repair and for valve annuloplasty.
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Person standing on Bodyport scale in bathroom

Bodyport claims FDA clearance for cardiac weight scale

Aug. 9, 2022
By Catherine Longworth
The U.S. FDA granted digital therapeutics company Bodyport Inc. 510(k) clearance for its heart monitoring weight scale. The digital solution includes sensors and algorithms that measure hemodynamic biomarkers to assess heart function and fluid status when patients take their daily weight. San Francisco-based Bodyport told BioWorld the platform is for heart failure (HF) patients in the U.S.
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Massive cell-free DNA trial for the detection of cancer completes enrollment

Aug. 9, 2022
By Nuala Moran
The largest study to date assessing the use of cell-free DNA (cfDNA) analysis to detect cancer in advance of symptoms has completed enrollment of 140,000 healthy volunteers. The study, being run in the U.K. National Health Service (NHS) by the charity Cancer Research UK (CRUK) and cfDNA diagnostics specialist Grail Inc., is using Grail’s Galleri test to look for cancer-specific methylation patterns in blood.
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Regulatory actions for Aug. 9, 2022

Aug. 9, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Avenda, Bodyport, Bot Image, Cerevasc, Imspex Diagnostics, Medalliance, Neuroone.
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