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BioWorld - Tuesday, January 27, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

April 6, 2023

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3D illustration of kidney cross section

Launch of Mozarc Medical strikes a chord for patients with kidney failure

Medtronic plc and Davita Inc. launched a new company this week centered on the assets and capabilities of Medtronic’s former Renal Care Solutions (RCS) division. Mozarc Medical US LLC brings Medtronic’s strategic plan to streamline its operations by spinning off several divisions one step closer to fruition. Read More

Bain pumps $215M into Heartflow as series F lead investor

Heartflow Inc. is feeling the love of investors again as it closed a $215 series F financing round led by Bain Capital Life Sciences. The round marks a return to the equity markets after several years away; the company closed its series E in 2017 and a $65 million venture round in 2019. In early 2022, Heartflow scrapped its plans to go public through a special purchase acquisition company (SPAC) merger with Longview Acquisition, citing what both companies called “current unfavorable market conditions.” Longview had offered $690 million in July 2021, in a deal that implied an enterprise value of $2.4 billion at the time. Read More
AI_landscape.png

Owkin leads €33M cancer fighting AI project in France

Okwin Inc. is leading a consortium of hospitals and pathology labs from across France as part of a €33 million (US$36 million) project to develop and deploy new digital pathology artificial intelligence (AI) tools to improve cancer care. The project, called Portrait, is backed by the French government, and the hope is that by producing more efficient and accessible diagnostic tools, clinicians will be able to better tailor treatments to individual patients at an earlier stage of the disease. Read More

FDA retains ‘handling’ in device animal studies final guidance

The U.S. FDA has wrapped up an October 2015 draft guidance for animal studies for medical devices, which prompted some lengthy responses from stakeholders concerned about some unique terms, such as device “handling.” Despite industrial opposition to the inclusion of that term, the final guidance retains the term handling and defines it in part as the manner in which the device “responds to the demands of the operator,” a term that may or may not be encompassed by the FDA’s overarching policy for human factors engineering. Read More
Freestyle Libre 3 sensor with smartphone app

Abbott warns against use of non-proprietary charging cables for Freestyle Libre

Batteries used in medical devices don’t always perform as expected, but Abbott Laboratories has issued an advisory to users of its Freestyle glucose monitoring systems in connection with overheating of the batteries used in the device’s readers, a problem the company said is not related to the batteries themselves. Abbott Park, Ill.-based Abbott has received reports of battery swelling and overheating in the reader unit, but advised users that use of non-Abbott charging cables seems to drive the risk of such episodes, urging users to stick with the USB charging cables that came with the readers. Read More
Fibroscan - Echosens

Echosens gets FDA clearance to expand use of its comprehensive liver management technology

Echosens SA obtained clearance from the U.S. FDA to expand the indications for screening with its Fibroscan system. The approval removes contraindications for pregnancy and active implant and includes patients with confirmed or suspected liver disease. It designates Fibroscan as a noninvasive aid for clinical management, diagnosis and monitoring of adult and pediatric patients with liver diseases. The age has been removed as the first selection probe and exam-type step. Read More
High Flux Reactor in the Netherlands

Radiopharma industry grapples with supply challenges

Radiopharmaceuticals require sophisticated infrastructure, with just-in-time radioactives delivered to patients who must isolate while receiving the therapy. Quality control and numerous layers of regulation makes for a daunting space to enter. Although the demand for medical isotopes is growing, the facilities that can make these products are aging, and one of the major facilities globally has already come offline. Next steps for the industry will be to solve supply and regulatory challenges as clinical trial data start to differentiate therapies in the pipeline. Read More

How are radiopharma companies managing supply challenges?

Supply issues are a “major concern for the whole industry and for the medical community as well, because they see targeted radiotherapy as a very promising field with very interesting results in the clinic, but they are concerned that drugs may not be available for a large number of patients, and it is a legitimate concern,” Orano Med SAS CEO Julien Dodet said. Companies such as Orano, Fusion Pharmaceuticals Inc. and Telix Pharmaceuticals Ltd. are working to meet those supply challenges. Read More

BioWorld MedTech Patent Highlights: Week 13

BioWorld MedTech presents Patent Highlights, an excerpt of the most important med-tech patents from this week's Cortellis Patents Gazette. Read More

Holiday notice

BioWorld's offices will be closed in observance of Good Friday. No issue will be published April 7. Read More

Appointments and advancements for April 6, 2023

New hires and promotions in the med-tech industry, including: Evoendo, Ora. Read More

In the clinic for April 6, 2023

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

Other news to note for April 6, 2023

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aiosyn, Electrocore, Lumiradx, Pathomation. Read More

Regulatory actions for April 6, 2023

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Edap Tms, Icentia, Restor3d. Read More

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