Anorganic Cancellous Bone Granules — Natural Hydroxyapatite for Predictable Bone Regeneration
InterOss® is a natural hydroxyapatite bone grafting material made from a proven multi-step purification process, leaving only a pure bone mineral composition. Chemically and structurally comparable to mineralised human bone, it features an interconnected network of macro and micro pores that create an ideal environment for cell attachment, vascularisation, and new bone formation. Available in sterilised granule form in vials and syringes for single use.
Download Product Brochure (PDF)*Histomorphometry data from comparative preclinical study (InterOss® vs Bio-Oss®). Not statistically significant.
InterOss® combines the proven osteoconductive properties of natural bovine hydroxyapatite with a unique pore structure that closely mimics human cancellous bone — creating the ideal biological scaffold.
InterOss® — Anorganic Cancellous Granules
InterOss® is indicated across the full spectrum of bone regeneration procedures in implant, periodontal, and oral surgery.
Augmentation or reconstructive treatment of the alveolar ridge, including filling of extraction sockets to maintain ridge volume for future implant placement.
Filling of infrabony periodontal defects in conjunction with products intended for guided tissue regeneration (GTR) and guided bone regeneration (GBR).
Elevation of the maxillary sinus floor (lateral window or crestal approach) to provide sufficient bone height and volume for implant placement in the posterior maxilla.
Filling of peri-implant defects in conjunction with guided bone regeneration products — supporting osseointegration around implants in compromised sites.
Filling of defects following root resection, apicoectomy, and cystectomy — where precise, stable graft placement is required for predictable healing.
Horizontal and vertical ridge augmentation procedures, used alone or in combination with autologous bone or allograft, with or without a collagen membrane barrier.
Hydrate InterOss® granules in blood or sterile saline solution prior to placement for optimal consistency and handling.
Administer to the surgical site using a surgical currette or periosteal elevator. Ensure the graft material makes sufficient contact with the bleeding bone surface to facilitate ingrowth of new blood vessels and bone-forming cells.
A resorbable membrane (such as InterCollagen® Guide) should be placed over the graft material to minimise particulate migration and guide bone regeneration.
Ensure that the grafted site is securely closed with soft tissue free of tension to support undisturbed healing and graft stability.
Allow at least 6 months of healing before re-entry to ensure complete graft integration. Healing time varies by defect size and patient biology.
Download the complete InterOss® GBR Materials brochure — full product specifications, indications, application protocol, comparative clinical data, granule size options, and clinical case studies from leading dental institutions.
Download Brochure — FreeGet pricing, availability, and clinical support for InterOss® granules in India. Our team is available Mon–Sat, 9:30 AM – 7:00 PM from Bengaluru.
