SBIR program renewed, but NIH's strict security rules may hurt medtech funding. President Trump signed S. 3971 on April 13, ...

Edwards Lifesciences secures FDA clearance for its ECLIPTIS Left Atrial Appendage Exclusion System, entering a competitive ...

MD+DI Senior Editor Amanda Pedersen takes a close look at the trend of partnerships and collaborations in the medical device ...

Medtronic's 2026 acquisition strategy aligns with its recent hiring of a veteran J&J exec as the company's first-ever CFO of ...

Medline recalls over 7,000 cardiac procedure kits due to contaminated anesthetic injections.The recall is the latest in a ...

This is the latest bid in a prolonged strategic review process that has seen the company reject previous acquisition ...

Research shows a new procedure, genicular artery embolization (GAE) could provide a viable alternative to knee replacement ...

Mary Lou Jepsen is the founder of Openwater, which is building optical and ultrasound-based imaging and therapeutic platforms ...

Penumbra secured FDA clearance and CE Mark for THUNDERBOLT, the first computer-assisted vacuum thrombectomy device for stroke ...

FDA has closed its July 2025 warning letter to wearable fitness tracker maker Whoop regarding the company's Blood Pressure ...

FDA issued a warning letter to Zoll Medical following a 14-month inspection of its Chelmsford, Massachusetts facility.

FDA warns against unapproved SNOO sleep sacks after finding safety risks, unauthorized hospital use, and quality failures at ...