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BONESUPPORT

Ownership: Private
Development stage: Commercial

Overview

BONESUPPORT has commercialized several synthetic injectable bioceramic bone graft substitutes under the CERAMENT brand. These products have demonstrated effective remodeling to host bone within 6–12 months. CERAMENT G has been recognized as a breakthrough device by the FDA and approved in Europe since 2013. The company’s clinical studies support use in trauma, infection-related defects, and other orthopedic indications.

Therapeutic areas: OtherEndocrinologyRheumatologyInfectious Diseases
Modalities: DeviceBiologic (bioceramic bone graft substitute)Drug-eluting device
Industry: Surgical Medical Devices

Drug pipeline

2 assets

CERAMENT BONE VOID FILLER

Commercial

Indications: Bone defects, Bone voids

1 more asset in the full pipeline.

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Partnerships

Former distribution agreement with ZimmerBiomet for US/Canada distribution of Cerament line until May 2018.Current network of independent distributors post-ZimmerBiomet agreement termination.

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