Centinel Spine Secures EU MDR Certification for prodisc C Vivo and C Nova Systems

Centinel Spine has received European Union Medical Device Regulation (EU MDR) certification for its prodisc C Vivo and prodisc C Nova cervical total disc replacement (TDR) systems. Following completion of registration and certification, both products are now CE-marked, confirming compliance with the latest European regulatory standards.

In global clinical use since 2009, the prodisc C Vivo features keel-less insertion and an anatomically shaped superior endplate with lateral spikes for optimal fit and immediate fixation. The prodisc C Nova, meanwhile, incorporates a flat endplate for flat vertebral anatomy and a tri-keel design to ensure stability. Both devices leverage prodisc CORE technology, which has demonstrated consistent clinical outcomes in more than 275,000 implantations over 35 years.

Centinel Spine remains dedicated to advancing solutions for cervical and lumbar spinal disorders. In 2023, Silony Medical International acquired Centinel Spine’s global fusion business to expand into the US spinal fusion market.

15-09-2025