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BioWorld - Tuesday, February 10, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Dec. 5, 2025

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Blue test tubes and dropper

Natera envisions cancer-testing future with $450M Foresight buy

Natera Inc. completed the acquisition of Foresight Diagnostics Inc. in a deal structured as $275 million up front plus contingent payments of up to $175 million based on achieving certain milestones for revenue and reimbursement coverage. The companies expect to close the transaction in the second quarter of 2026. Read More
Invest compass

Cancer blood test maker Freenome going public with $330M SPAC

Freenome Holdings Inc. reported it is going public via a special purpose acquisition company. The company said it expects to raise $330 million, which it plans to use for the 2026 launch of its blood-based screening tests for multiple cancers. Backed by an affiliate of Perceptive Advisors - Perceptive Capital Solutions Corp. (PCSP) – and joined by RA Capital, the arrangement includes a commitment of $240 million in equity investments plus about $90 million more held by the SPAC’s trust fund. Other notable investors, including ADAR1 Capital, Bain Capital Life Sciences, and Farallon Capital Management have signed on to participate in the deal.
Read More
Boston Scientific Rezum

Boston Sci brings next-generation Rezūm EVO Console to the UK

The first procedure to treat benign prostatic hyperplasia with Boston Scientific Corp.’s next-generation Rezūm EVO Console was successfully completed in the U.K. The device, which recently received CE mark, is intended to be used with the Rezūm Water Vapor Therapy, a minimally invasive treatment that uses water vapor to reduce prostate tissue. Read More
regulatory-washington-capital.png

FDA’s use of generalist field investigators creating new dilemmas

The U.S. FDA’s recent switch toward more routine use of generalist field investigators might be seen in some quarters as an attempt to do more with less, but a session on the topic at the Food and Drug Law Institute’s annual enforcement conference in Washington seems to suggest that this reversal of historic practice presents at least as many problems as solutions for industry. Read More
Vial and syringe with blue hues

Hippocratic loath? ‘Harm’ threat from ACIP’s proposed HBV shift

Individual liberty and choice vs. wider public health became one predictable hinge upon which swung the often-acerbic debates at the CDC’s Advisory Committee for Immunization Practices (ACIP) meeting, which took up – again – the matter of hepatitis B virus (HBV) vaccine scheduling, a day after the panel voted not to vote on such guidance. Read More
Tracy Beth Høeg, acting CDER director

Høeg appointment as acting CDER director tied to vaccine strategy?

After a more than 13-year period of stability with Janet Woodcock as the head of CDER, with Patrizia Cavazzoni taking charge during the next four years of former U.S. President Joe Biden’s tenure, the FDA division has had no fewer than five different people in charge throughout 2025. Up to bat now as acting director is Tracy Beth Høeg, a physician and epidemiologist who co-authored a paper in 2022 with CBER Director Vinay Prasad, FDA Commissioner Marty Makary and others demonstrating that COVID-19 boosters and college vaccine mandates were harmful to young men due to myocarditis risks. Read More

Appointments and advancements for Dec. 5, 2025

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

Other news to note for Dec. 5, 2025

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Conmed, Icecure, Medirom, Olympus, Seegene, TD Synnex, Tenon, WL Gore. Read More

Regulatory actions for Dec. 5, 2025

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Atraverse, Cardiawave, Medtronic. Read More

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