Spineart Announces FDA Approval of BAGUERA® C Cervical Disc

GENEVA, Aug. 11, 2026 /PRNewswire/ -- Spineart announces that the BAGUERA® C cervical disc has received FDA approval for 1 and 2 contiguous levels, expanding access in the United States to a motion-preserving solution for patients suffering from cervical disc disease.

As one of Spineart’s foundational technologies and a cornerstone of its cervical portfolio, BAGUERA® C brings nearly two decades of international clinical experience to a market with relatively few cervical disc replacement options. Since its introduction, over 80,000 devices have been sold worldwide, establishing a long track record of clinical use.

The FDA approval is supported by two randomized controlled trials with nearly 600 patients enrolled in the United States. Additional clinical evidence, including a 10-year follow-up study published in The European Spine Journal in 2023, demonstrated that 85% of implants maintained motion a decade after treatment, providing long-term data on preservation of motion at the treated level.

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