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14 Apr 25
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14 Apr 25

NanoBone® SBX Putty and NanoBone® QD’s indications expanded to include interbody spinal fusion in the US

NanoBone can now be used in intervertebral body fusions with an intervertebral body fusion device cleared by the FDA

Keele, UK, 14 Apr 2025 – Biocomposites is thrilled to announce that NanoBone® SBX Putty and NanoBone® QD’s indications have been expanded to include interbody spinal fusion in the US. NanoBone can now be used in intervertebral body fusions with an intervertebral body fusion device cleared by the FDA.

NanoBone is a synthetic, ready-to-use bone graft substitute, utilizing nanostructured HA and silica that enables osteogenesis in the first 10 days. It is preloaded, versatile, ready-to-use and provides:

🟣Comparable healing rate to autograft
🟣Rapid absorption and reliable bone fusion
🟣Early osteogenesis
🟣Patented nanostructure and optimized composition

We are happy to continue to expand our indications and help more patients achieve better outcomes.

Contact for Media enquiries

Optimum Strategic Communications
Mary Clark, Stephen Adams, Katie Flint
Tel: +44 (0)20 3882 9621
biocomposites@optimumcomms.com

About Biocomposites

Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries. Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world. Please visit biocomposites.com to learn more.

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