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BioWorld - Sunday, February 15, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Jan. 24, 2022

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Intellis device image

With FDA approval, Medtronic challenges Nevro in PDN market

Medtronic plc received FDA premarket approval Friday for use of its Intellis rechargeable and Vanta recharge-free neurostimulators in patients with diabetic peripheral neuropathy (DPN), suddenly tripling the number of spinal cord stimulators approved for the indication. Medtronic’s implantable spinal cord stimulators (SCS) now join Nevro Corp.’s HFX, which has had the distinction since July 2021 of being the only device with FDA approval for DPN, also known as painful diabetic neuropathy (PDN). Read More
Royal Philips headquarters

Philips says supply chain troubles hampering growth

Supply chain issues overshadowed Royal Phillips NV fourth-quarter 2021 results, as the Dutch conglomerate reported sales of $5.5 billion (€4.9 billion), a 10% organic year-on-year decline. Philips management said sales were impacted by several headwinds, including supply chain challenges and postponement of equipment installations in hospitals related to COVID-19. The recall of the Respironics device also caused a double-digit decline in the sleep & respiratory business. Read More
U.K. flag on stethoscope

NICE set to expand scope of HTAs, but industry still sees gaps

LONDON – The industry is expressing divergent views of changes to how the U.K. health technology assessment agency, the National Institute for Health and Care Excellence (NICE), will in the future select what products to assess and the methods and processes it will use to carry out its evaluations. Read More
cloud-cybersecurity.png

IV pumps top list of medical devices still vulnerable to cybersecurity threats

Cybersecurity challenges can represent an existential threat to patients on medical devices, and a new report by New York-based Cynerio Inc. highlights some of those challenges. One of the findings in the report is that nearly three-fourths of intravenous pumps, which make up 38% of a hospital’s internet of things (IoT) footprint, are vulnerable to an attack, a predicament that continues to put desperately ill patients in jeopardy. Read More
Laptop displaying FDA logo

FDA reports recall of Medtronic Hawk One atherectomy device

The FDA announced a class I recall of the Medtronic Hawk One directional atherectomy catheter system due to more than 160 reports of problems with the device’s guidewire. The catheter tip could break or separate when the guidewire prolapses, a problem that is associated with 55 injuries and no deaths, but the recall affects more than 95,000 units. Read More

Appointments and advancements for Jan. 24, 2022

New hires and promotions in the med-tech industry, including: Activ Surgical, DCN Dx, Idbydna, Intervenn, Think Surgical. Read More

Financings for Jan. 24, 2022

Med-tech firms raising money in public or private financings, including: Dnovo, Seqone Genomics. Read More

In the clinic for Jan. 24, 2022

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

Other news to note for Jan. 24, 2022

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Coagco, Exactech, Illumina, Jointmedica, Medtech Solutions, Nanovibronix, North American Rescue, Optina. Read More

Regulatory actions for Jan. 24, 2022

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Magnesium Development. Read More

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