LDR Cervical Disc Replacement Gains FDA Approval

Austin, Texas-based LDR received FDA approval for the commercial sale and distribution of the Mobi-C Cervical Disc for one-level indications.

Advertisement

The Mobi-C is made of cobalt chromium alloy and polyethylene. It is designed as a bone-sparing, cervical intervertebral disc replacement. It has shown non-inferiority in trial success compared to the standard ACDF treatment.

The pre-market application for two-level device use is currently under review.

More Articles on Devices:
Steven Epstein Named to OrthoSensor Board of Directors
Renaissance Spine Sales Boost Mazor Robotics’ Gross Profits 130%
12 Spine Devices Receive FDA 510(k) Clearance in July

 

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Spinal Tech

  • From new technology acquisitions to regulatory clearances to leadership changes, here are 20 developments and updates from the biggest players…

  • SurGenTec’s ION-C earned FDA 510(k) clearance for ION-C navigation instruments with the ION-C posterior cervical facet fixation implant, according to…

  • VB Spine has made big pushes into the spine medtech space so far in 2026, including global expansions. Six headlines…

Advertisement

Comments are closed.