The AccuStride System is intended to enhance surgical outcomes for proximal phalanx and metatarsal arthroplasty.

Sibel Health announces the close of new $30 million dollar Series C financing round led by the Steele Foundation for Hope ...

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 ...

Ben Sexson, Monogram Chief Executive Officer, commented, "This FDA 510(k) clearance is a defining moment for Monogram. It marks the culmination of years of relentless effort, innovation, and teamwork.

HENDERSON, Nev., March 25, 2025 /PRNewswire/ -- Restore Robotics is pleased to announce it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for remanufacturing Da ...

The Dawes-Redman CTG Analysis is designed to assess if a non-stress test trace meets the “criteria of normality".

MedCAD has received 510(k) clearance from the US Food and Drug Administration (FDA) for its AccuStride Foot and Ankle System. This clearance permits the company to provide surgeons with patient ...

Ben Sexson, Monogram Chief Executive Officer, commented, "This FDA 510(k) clearance is a defining moment for Monogram. It marks the culmination of years of relentless effort, innovation ...