DirectOss Anorganic Cancellous Xenograft Granules Size: 0.25mm-1mm (1g)

Description:

DirectOss Anorganic Cancellous Xenograft Granules are a bovine-derived mineralized bone material designed for appropriate dental bone augmentation procedures. This configuration contains 0.25-1mm particulate material with a 1g quantity supplied in one vial per box. The manufacturer identifies DirectOss as an anorganic bone mineral matrix comparable in structure to human bone. The material is described as a bovine hydroxyapatite cancellous xenograft and is derived from Australian bovine bone identified by the manufacturer as BSE-free. DirectOss has hydrophilic properties that allow it to absorb the patient's blood, while its interconnected macro- and microporous structure and large internal surface area are described as providing an environment for cell attachment and bone growth.

The 0.25-1mm particulate size provides a defined granule range that can be considered when selecting a graft material for an appropriate procedure. The 1g vial provides a larger quantity than the 0.25g configuration and may be selected according to the treatment site's requirements and the amount of material needed. The manufacturer lists the product for horizontal or vertical augmentation procedures. Dental professionals should evaluate the clinical site, desired augmentation, defect dimensions, grafting plan, and applicable product labeling before selecting the appropriate volume and particle size. Proper handling and placement should follow the manufacturer's instructions for use and established clinical protocols.

DirectOss is part of the Implant Direct biomaterials portfolio and is available in multiple quantities, allowing dental teams to select a configuration that matches procedural requirements. The vial format supports organized storage and preparation of the graft material before use. Dental professionals should verify the product name, particulate size, quantity, and packaging before opening the sterile product for a procedure. The material should be used only for its labeled purpose and by appropriately trained professionals. Clinicians should review current instructions for use, indications, contraindications, warnings, precautions, storage requirements, and handling instructions before use. Patient-specific factors and professional clinical judgment should always guide graft material selection and application.