“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 ...

Aurora Spine Corporation ("Aurora Spine" or the "Company") (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain management ...

Intelligent Bio Solutions Inc. (Nasdaq: INBS) ("INBS" or the "Company"), a medical technology company delivering intelligent, rapid, non-invasive testing ...

Restore Robotics is pleased to announce it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for ...

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 ...

The new framework is intended to make postmarket changes easier for products. Experts recommend having a clear roadmap and contacting regulators early.

Intelligent Bio Solutions Inc. (Nasdaq: INBS) ("INBS” or the "Company”), a medical technology company delivering intelligent, rapid, non-invasive testing solutions, today provided shareholders with a ...

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 ...