Silicate-Enriched Granules have been developed to support the bone healing process in dental applications, thanks to their highly porous structure and biocompatible, sterile formulation.
Indications Handling Tips Specifications
Powerbone Silicate-Enriched Granules support initial clot stabilization with their highly porous structure. Their calcium phosphate content, which has a composition similar to the mineral component of natural bone, provides a conductive scaffold for blood vessels and bone-stimulating cells. Powerbone graft materials acquire bioactive properties thanks to their silica content, which enhances protein retention in the circulation.
• This product must be used under sterile conditions and only by healthcare professionals.
• Before use, check the packaging for integrity and verify the expiration date.
• The defect site must be properly prepared and cleaned.
• The granules can be applied directly or moistened with appropriate sterile solutions.
• The graft material should be placed in the defect area without excessive compression.
• Stabilization with a membrane may be used when necessary.
• This product is for single-use only; it must not be re-sterilized or reused.
• This product must be used under sterile conditions and only by healthcare professionals.
• Before use, check the packaging for integrity and verify the expiration date.
• The defect site must be properly prepared and cleaned.
• The granules can be applied directly or moistened with appropriate sterile solutions.
• The graft material should be placed in the defect area without excessive compression.
• Stabilization with a membrane may be used when necessary.
• This product is for single-use only; it must not be re-sterilized or reused.
• This product must be used under sterile conditions and only by healthcare professionals.
• Before use, check the packaging for integrity and verify the expiration date.
• The defect site must be properly prepared and cleaned.
• The granules can be applied directly or moistened with appropriate sterile solutions.
• The graft material should be placed in the defect area without excessive compression.
• Stabilization with a membrane may be used when necessary.
• This product is for single-use only; it must not be re-sterilized or reused.
