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BioWorld - Saturday, June 13, 2026
Home » Topics » Medical technology

Medical technology
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Nephrodite Holly

Nephrodite's Holly renal replacement named breakthrough device

Dec. 15, 2025
By Annette Boyle
Nephrodite Inc.'s Holly, an implantable, continuous renal replacement system, received U.S. FDA breakthrough device designation as a novel and potentially life-changing treatment for end-stage kidney disease. The system is designed to enable continuous blood filtration and allow patients freedom to go about their days without frequent, hours-long visits to a dialysis clinic or being hooked up to a filtration system at home.
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Illustration of human anatomy, enlarged prostate

Proverum, Zenflow secure FDA nod for systems to treat BPH

Dec. 15, 2025
By Shani Alexander
The U.S. FDA recently cleared two new medical devices to treat benign prostatic hyperplasia, offering men with enlarged prostates additional treatment options which are minimally invasive. The approvals include Proverum Medical Ltd.’s Provee System and Zenflow Inc.’s Zenflow Spring Implant and Delivery System, both are first-line interventional therapeutic options which offer relief to the millions of men living with the condition.
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Appointments and advancements for Dec. 15, 2025

Dec. 15, 2025
New hires and promotions in the med-tech industry, including: Envue Medical.
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Financings for Dec. 15, 2025

Dec. 15, 2025
Med-tech firms raising money in public or private financings, including: Inspira Technologies, Impulse Dynamics.
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In the clinic for Dec. 15, 2025

Dec. 15, 2025
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Radiopharm Theranostics.
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Other news to note for Dec. 15, 2025

Dec. 15, 2025
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bioretec, Heartsciences, Helio Genomics, Lunit, Natera, Neogenomics, Neurosigma, Philips, Spectrawave.
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Regulatory actions for Dec. 15, 2025

Dec. 15, 2025
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Companion Spine, Hyperfine.
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CT scan of brain showing subdural hematoma

FDA greenlights Medtronic Onyx subdural hematoma treatment

Dec. 12, 2025
By Annette Boyle
Sometimes the darkest products (names) bring a bright spot of news to their developers, as the U.S. FDA clearance for Galway, Ireland-based Medtronic plc's Onyx liquid embolic system demonstrates. Onyx gained the indication for embolization of the middle meningeal artery as an adjunct to surgery for the treatment of symptomatic subacute or chronic subdural hematoma based on the EMBOLISE trial results. The approval represents a significant advancement in treating this common neurosurgical condition.
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Ebenbuild technology lung with ARDS

Ebenbuild aims to transform lung care with digital twin tech

Dec. 12, 2025
By Shani Alexander
Ebenbuild GmbH is hoping that its digital twin technology platform that combines AI and physics-based computational models tailored to individual patients will transform respiratory care. From drug development to optimizing mechanical ventilation in critical care, the company’s software-based solutions aim to reveal what is happening in the ‘black box’ of the lungs, helping clinicians to improve outcomes and reduce mortality.
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Line graph arrow trending upward

November reignites med-tech momentum with $4.7B raised

Dec. 12, 2025
By Amanda Lanier
Med-tech financing activity from January through November 2025 reached $31.32 billion, marking a strong rebound from the sector’s lows in 2023 to 2024, which saw $16.61 billion and $23.64 billion in the same period, respectively. While still far below the capital inflows seen in 2020 and 2021, when the first 11 months of the year exceeded $48 billion, the steady upward progression over recent years suggests renewed investor engagement and improving capital availability. In November, $4.73 billion was collected through 36 transactions, up from $3.25 billion in October.
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