6 Orthobiologic Companies Move Clinical Trials Forward
Multiple orthobiologic companies have engaged in clinical trials in 2019, seeking to demonstrate the efficacy of their cell-based products. We've...
Multiple orthobiologic companies have engaged in clinical trials in 2019, seeking to demonstrate the efficacy of their cell-based products. We've...
The JOURNEY II Uni Knee is designed to bring the natural feel of JOURNEY II to partial knee arthroplasty patients...
Enrollment is complete in the investigational arm of the U.S. IDE trial of the LimiFlex Paraspinous Tension Band with decompression....
Momentum is compatible with the company's neon3 Universal OCT Spinal Stabilization System, which launched in 2012....
Carmell Therapeutics' proprietary process binds and cross-links regenerative factors in lyophilized platelet-enriched plasma into solid and semi-solid plasma-based materials to...
Small and mid-sized orthopedic companies bolstered their portfolios at year-end with products to help grow revenue in the coming year....
In the race to capitalize on patient-driven interest in stem cells, biologic and regenerative solutions, there has been an explosion...
Dr. Steven Sampson, Founder of the well-known TOBI Symposium, shares his take on the state of regenerative medicine and the...
Spine implants accounted for the majority of the additive manufactured products that received FDA 510(k) clearance in 2019. Our review...
This month, we look at companies that received their first orthopedic-related clearance such as FX Shoulder USA, Amplify Surgical and...
The first of its kind biomaterial is offered as an alternative to PEEK and titanium materials for interbody devices....
OXINIUM Technology is the first advanced bearing material available to support modular dual mobility throughout the entire offering....
How should you prepare for FDA 510(k) submissions in 2020? Start with a thorough understanding of the testing and verification...
Together, the companies will jointly promote the rapid development of digital surgery and technological medical innovation, providing insights for the...
Stryker received FDA 510(k) clearance to market the SAHARA® Lateral 3D Expandable Interbody System featuring Lamellar 3D Titanium Technology. This...
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