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BioWorld - Friday, December 26, 2025
Home » Topics » Medical devices and technologies

Medical devices and technologies
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Canadian flag

Canada expands regs to protect drug, device supplies

Sep. 2, 2021
By Mari Serebrov
Even as the Biden administration pushes for drug imports from Canada as a way to help curb U.S. prescription drug prices, Canada is doubling down on its efforts to protect its supply of drugs and medical devices.
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U.S. flag and money

U.S. lawmakers look to failed drug pricing policies to fund $3.5T budget

Aug. 23, 2021
By Mari Serebrov
As the U.S. House of Representatives resumes work Aug. 23 on a budget reconciliation proposal to get a $3.5 trillion fiscal 2022 budget across the finish line, many lawmakers are looking to provisions to reduce prescription drug prices as a way to pay for increased spending in other health care sectors.
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Woman with mask using nasal spray

Virpax breathes easier with positive FDA comments as it joins the COVID-19 intranasal race

Aug. 20, 2021
By Lee Landenberger
The FDA’s pre-IND response to Virpax Pharmaceuticals Inc.’s MMS-019, a molecular masking spray being developed as an over-the-counter product to limit transmission of SARS and influenza, has the company breathing easier and ready to chase an NDA. Virpax is in a crowded field of 43 COVID-19 intranasal therapeutics and vaccine programs.
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Patent gears

Australian government unveils framework for a patent box to offset R&D for drugs and devices

Aug. 17, 2021
By Tamra Sami
PERTH, Australia – The Treasury Department is seeking feedback from industry stakeholders on its discussion paper on a patent box policy, which was first announced in the May 2021 federal budget.
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Patent gears

Australian government unveils framework for a patent box to offset R&D for drugs and devices

Aug. 13, 2021
By Tamra Sami
PERTH, Australia – The Treasury Department is seeking feedback from industry stakeholders on its discussion paper on a patent box policy, which was first announced in the May 2021 federal budget.
Read More
10-28-Boston-Science_Global-Headquarters_Marlborough,-Mass

Boston Scientific recalls Ingenio devices due to faulty transition to safety mode

Aug. 10, 2021
By Mark McCarty
The FDA reported that Boston Scientific Corp. has recalled several models from the Ingenio line of cardiac electrophysiology devices in a class I action that affects 48,000 devices. The recall was triggered by the risk that these devices will inappropriately shift into safety mode and thus be unable to provide pacing, as demonstrated by 65 such incidents and three instances in which patients needed external pacing in response to the problem.
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Graphene illustration

Graphene coating may prevent the formation of biofilms on medical implants

Aug. 10, 2021
By Nuala Moran
LONDON – Swedish researchers have devised a method for binding insoluble antibiotics to graphene coatings, in an advance that could prevent the formation of biofilms on medical implants. In comparison to other long-winded methods for loading antibiotics onto implant surfaces, they say the way in which they bind active molecules to graphene is simple and could easily be integrated into manufacturing processes.
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Gavel and scales

Appeals court affirms Life Spine’s injunction against L&K Biomed for Prolift device

Aug. 10, 2021
By Mark McCarty
The U.S. Court of Appeals for the Seventh Circuit has affirmed an injunction obtained by Life Spine Inc. against L&K Biomed for the latter’s alleged appropriation of trade secrets obtained by an L&K subsidiary. The outcome affirms that injunctive relief is available to plaintiffs when irreparable harm is plausibly alleged, but also highlights the need for internal controls to avoid accidental use of trade secrets during product development programs.
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Nanox.Arc

Nanox reimagines radiology with two acquisitions

Aug. 10, 2021
By Annette Boyle
Continuing its push to streamline the imaging industry from equipment to vertical integration, Nano-x Imaging Ltd. (Nanox) agreed to acquire Zebra Medical Vision Ltd. and signed a letter of intent to buy Usarad Holding Inc. and its related company Medical Diagnostics Web. The timing of the transactions, designed to create an end-to-end radiology solution, was not announced.
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FDA: Imaging agents to transition from drugs to devices

Aug. 10, 2021
By Mari Serebrov
Rather than appeal an April decision by the U.S. Court of Appeals for the District of Columbia Circuit, the FDA is changing how it regulates imaging agents. That means the agency will transition at least some approved imaging agents from drug status to device status and, going forward, it will regulate products that meet both the device and drug definition as devices – unless Congress specifies otherwise.
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