A debilitating condition affecting 1 in 4 women is desperately crying out for a solution, and the next generation of treatments to repair the damage of pelvic organ prolapse (POP) has just come a big step closer.

They combined a blend of slimy and sticky proteins to produce a fast-acting, bacteria-blocking, waterproof adhesive for use in biomedical applications.

Boston Scientific (NYSE: BSX)+
announced today that it received CE mark for its navigation-enabled Farawave Nav ablation catheter and Faraview software.

MELBOURNE, Australia, Feb. 16, 2025 /PRNewswire/ — Navi Medical Technologies, a medical device company focused on pediatric healthcare innovation, proudly announces that its Neonav® ECG Tip Location System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA).

TAMPERE, Finland, Feb. 14, 2025 /PRNewswire/ — Bioretec Ltd., a pioneer in absorbable orthopedic implants, has achieved a pivotal milestone with the successful completion of its CE mark approval process for the RemeOs™ Trauma Screw product portfolio

A Medtronic (NYSE: MDT)+
official said today on LinkedIn that the company won CE mark for its Crescent RA jugular dual lumen catheter.

Accelus this week announced its FlareHawk Interbody Fusion System received regulatory approval in Brazil.

JAMA today published outcomes from a study evaluating the safety and efficacy of the Insulet Omnipod 5 in adults with type 2 diabetes.