Julie A. Vetalice, Author at ORTHOWORLD

Waldemar LINK Receives FDA 510(k) Clearance for CORE Shoulder System

Waldemar LINK Earns 510(k) for CORE Shoulder System

CORE is designed to assist in the placement of the K-wire for the glenoid component during total shoulder replacement.

Jun 30, 2025

CGBio Launches Novomax Fusion in Japan

The third-generation cervical spine cage utilizes BGS-7, a new bioactive glass-ceramic material, that may be more biocompatible than titanium or PEEK cages.

Jun 30, 2025

Carlsmed Announces Filing of Registration Statement for Proposed Initial Public Offering

Carlsmed Files Statement for Proposed Initial Public Offering

Investments The Numbers

The company's aprevo Technology Platform combines proprietary AI-driven software with patient-specific fusion devices to personalize surgical procedures, improve patient outcomes and reduce complications.

Jun 27, 2025

OssDsign Shares Update on PROPEL Spinal Fusion Study

Orthobiologics ORTHOFLASH

Results show a fusion rate of 88.4% in a highly complex patient cohort, demonstrating that Catalyst nanosynthetic bone graft shows strong performance even in challenging patient populations.

Jun 27, 2025

Stryker receives FDA clearance for Incompass Total Ankle

Stryker Granted FDA Clearance for Incompass Total Ankle

Joint Replacement ORTHOFLASH

Incompass incorporates Adaptis Boney Ingrowth Technology and redesigned instrumentation to support long-term fixation, surgical flexibility and streamlined workflow.

Jun 25, 2025