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ArthroCare, a maker of minimally invasive surgical products, has received FDA clearance for its second-generation Parallax Contour-enhanced vertebral augmentation device, according to a news release.

Please provide your email address to receive an email when new articles are posted on . Published results showed a significant proportion of patients with vertebral compression fractures had decreased ...

VySpine’s VyBrate VBR system earned the FDA’s 510(k) clearance, according to a Jan. 13 news release. The device combines the osseointegration properties of the OXPEKK material and the OsteoVy lattice ...

FDA clearance confirms robust safety and performance of VCFix® Spinal System, a breakthrough treatment for vertebral compression fractures US commercial pilot launch planned for early 2026, followed ...

NEW YORK--(BUSINESS WIRE)--AgNovos Healthcare, a developer of medical technology products leveraging regenerative medicine to treat the local effects of bone disease, announced today that its newest ...

OWINGS MILLS, Md., Aug. 25, 2020 /PRNewswire/ -- IZI Medical Products, LLC ("IZI"), a leading manufacturer of interventional radiology devices, announces the official launch of its Osteo-Site ...

- This data supports a strong safety profile for the VCFix(R) Spinal System for the treatment of vertebral compression fractures THE HAGUE, Netherlands, June 3, 2025 /PRNewswire/ -- Amber Implants, an ...

Discover the spinal implants and surgery devices market trends with our insightful analysis. Explore product types, technology, and surgery types for hospitals, specialty clinics, and ambulatory ...