Over 100 US Patients Treated in Catalyst Orthoscience and 3D-Side Collaboration ORTHOFLASH Robotics/Tech The platform includes anatomic and reverse planning capabilities that deliver an individualized surgical plan prior to the procedure. Jul 14, 2022
Onkos Surgical Gains 510(k) for Patient-Specific Pelvic Reconstruction System ORTHOFLASH Trauma This will expand Onkos' portfolio of musculoskeletal oncology and complex orthopedic solutions to include conditions of the pelvis. Jul 14, 2022
OrthoPediatrics Enters Distribution Agreement with 3D-Side Company Updates Competitive Landscape OrthoPediatrics will provide pre-op planning software and patient specific tools such as osteotomy and tumor resection cutting guides. Jul 13, 2022
LimaCorporate and Orthofix Medical Partner on High Hip Dislocation Device Company Updates Competitive Landscape The partnership combines the Fitbone intramedullary nail with a proprietary, patient specific 3D-printed pelvic fixation device. Jul 13, 2022
Expanded Indications for Bone Solutions Mg OSTEOINJECT Orthobiologics ORTHOFLASH Mg OSTEOINJECT is reportedly the first drillable, adhesive and injectable bone void filler in the U.S. to incorporate magnesium. Jul 13, 2022
FDA Accepts Empirical Spine’s Limiflex PMA Module II ORTHOFLASH Spine The LimiFlex DST is a first-of-its-kind surgical option for grade 1 degenerative spondylolisthesis patients with spinal stenosis. Jul 13, 2022
AlloSource Expands AlloConnex Line Orthobiologics ORTHOFLASH Theh company added a quadricep tendon to its AlloConnex line of tendons, ligaments and fascia. Jul 13, 2022
Orthox to Commence Trial of FibroFix Knee Cartilage Repair Orthobiologics ORTHOFLASH Orthox received permission in the UK to begin the "FFLEX Study" (derived from the "FibroFix cartiLage repair Experience"). Jul 13, 2022
Centinel Spine Gains FDA Approval for Additional prodisc Devices ORTHOFLASH Spine Centinel Spine now has four PMA-approved cervical total disc replacement devices. Jul 13, 2022
Aurora Spine Announces New FDA indication clearance of Lumbar Spinal Stenosis for its ZIPâ„¢ series of MIS implants ORTHOFLASH Spine FDA has cleared a new Lumbar Spinal Stenosis Indication for Aurora Spine's ZIP family of minimally invasive spinal implants. Jul 13, 2022