“Unlike traditional ACL reconstruction, which sacrifices healthy tissue and can lead to long-term issues like muscle weakness ...

Aurora Spine earned FDA 510(k) clearance for its Aero facet fusion system, the devicemaker said March 25. Aero is a minimally ...

In an agency first, the FDA has cleared a system designed to clean out the complex inner channels of flexible endoscopes—a ...

Tenon shares are moving higher on Tuesday on possible continued strength after the company announced yesterday that it ...

Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion, according to a March 24 news release. With the new indication Catamaran can ...

Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain management solutions, today announced that the U.S. Food and ...

Avant Technologies Inc. (OTCQB:AVAI) (”Avant” or the “Company”), and its partner, Ainnova Tech, Inc., (Ainnova), a leading healthcare technology company focused on revolutionizing early disease ...

Huntleigh Healthcare is proud to announce that the world-renowned Dawes-Redman CTG Analysis™ has been approved for use in the U.S.

Imperative Care announced FDA 510(k) clearance of its Symphony 16F 82cm catheter for venous thrombosis and announced the ...

Imperative Care, Inc. today announced U.S. Food and Drug Administration (FDA) 510(k) clearance of the 82cm version of its Symphony™ 16F Catheter, the company’s latest innovation designed to elevate ...