Elbow/Radial Head Replacement

Zimmer Biomet voluntarily recalled various legacy Biomet products due to cleaning processes that could lead to elevated bacterial endotoxin and residual debris.

Ignite Orthopedics received FDA 510(k) clearance to market a Radial Head Arthroplasty System, its first product to be cleared.

Stryker launched the ReUnion® S humeral stem, designed to be the ideal length to complement the ReUnion Shoulder Arthroplasty System.

The American Academy of Orthopaedic Surgeons launched the Shoulder and Elbow Registry in the U.S.

CurveBeam received CE Mark approval for LineUP and InReach, compact orthopaedic extremity CT systems.

Zimmer Biomet (ZBH) received FDA 510(k) clearance for compatibility of the Nexel™ Total Elbow with the Comprehensive® Segmental Revision System. This marks the 1st submission by ZBH to establish compatibility of two separate ZBH implant systems. 

Lima Corporate entered into an Innovation Alliance Agreement with the Hospital for Special Surgery. New product co-developments include a Trabecular Titanium total elbow and an advanced acetabular cup. 

At AAOS 2016, Exactech will unveil multiple revision arthroplasty devices for shoulder, knee and hip.