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BioWorld - Tuesday, December 16, 2025
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Oct. 16, 2024

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Novocure's Optune Lua

Novocure’s tumor treating fields land FDA approval for lung cancer

Novocure GmbH secured U.S. FDA approval for Optune Lua, a wearable device that delivers alternating electric fields or tumor treating fields that kill cancer cells. Indicated for use with PD-1/PD-L1 inhibitors or docetaxel in the second or subsequent line for the treatment of metastatic non-small-cell lung cancer following the failure of platinum-based regimens, the approval was driven by the significant improvement in overall survival rates seen in the LUNAR pivotal study for Optune Lua. Read More
Anovos miniature flexible robotic arms

FDA clears Momentis, CMR robotic systems

The U.S. FDA granted Momentis Surgical Ltd. 510(k) clearance for its Anovo robotic surgical platform for use in single site, abdominal access ventral hernia repairs. The U.S. regulatory agency also gave the greenlight to CMR Surgical Ltd.’s Versius system for use in cholecystectomy, in a sign of the growing market for smaller, more portable robotic devices to assist in minimally invasive procedures. Read More
AI biotech research concept with lightbulb and digital background

CBO scoring impedes expanded Medicare digital benefit categories

The U.S. Medicare program has a notorious problem with regard to coverage of digital products and software as a service, but the agency is dependent on Congress to add new benefit categories via legislation. Read More
EU flags

EU's MDR pain points exacerbated by lack of member state harmony

The saga of the EU's Medical Device Regulation (MDR) is far from over, but stakeholders were treated to another related dose of reality in a session at this year's Med Tech Conference here in Toronto. Several panelists pointed to a lack of harmonization regarding notified bodies' interpretation of the regulation, but Stryker Inc.'s Michel Marboeuf said this problem flows to some extent from a lack of harmonization among the member states' competent authorities, a condition that is likely to resist treatment in the near term. Read More
FDA-sign.png

US FDA Rare Disease Hub an answer to regulatory challenges?

Coming on the heels of an advisory committee in which the U.S. FDA and its independent advisers grappled with trying to fit an ultra-rare disease development program into the confines of the agency’s “significant evidence” requirements, an Oct. 16 public meeting on a Rare Disease Innovation Hub the agency is setting up seemed like a welcome step in the right direction for rare disease patients, their caregivers and companies working in the space. Read More

Appointments and advancements for October 16, 2024

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

Financings for October 16, 2024

Med-tech firms raising money in public or private financings, including: Ceribell, Ikerian. Read More

In the clinic for October 16, 2024

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

Other news to note for October 16, 2024

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 23andme, Atomvie Global Radiopharma, Bioaffinity, Brainscope, Codetta Bio, Conavi, Gilardoni, Jscreen, Myriad Genetics, Namsa, Paragonix, Precision X-Ray, Radiopharm Theranostics, Renovaro, RTI International, Terumo. Read More

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