Its expandable architecture allows the implant to pierce the ilium and sacrum, stabilizing the SI joint and enabling post-expansion graft delivery without disengaging the instrumentation.

IMPLANET and distribution partner Sanyou Medical have registered the JAZZ range, dedicated to tape fixation in the treatment of spinal pathologies, on the Chinese market.

THINK Surgical gained FDA 510(k) clearance for use of b-ONE Ortho’s MOBIO with TMINI in 2024.

Nanochon Chondrograft will be evaluated in a first in human study for use in knee cartilage restoration in eligible patients.

The trial will compare safety and effectiveness of Triadyme-C to ACDF in the treatment of symptomatic cervical disc disease.

The system supports treatment of scapular fractures using several different techniques, including single and dual plating.

VISIE’s scanning platform is completely non-invasive and employs no bone-pinned trackers, clamps or registration steps.

The novel device is designed to provide a minimally invasive option for patients suffering from facet joint-related pain or instability.

Highridge licensed U.S. rights to activL and is commencing production for the launch of its own activL lumbar disc later this year.

Of the more than 350 spinal bone grafts in the U.S. market, Cerapedics has two of only three spinal bone grafts that have successfully gone through the PMA process.