InterOss®

Anorganic Cancellous Bone Granules

InterOss

Description

InterOss® is a natural hydroxyapatite bone grafting material for use in dentistry. Made from a proven multi-step purification process which leaves only a bone composition, it is a highly purified osteoconductive material for bone regeneration.

Having an interconnected network of macro and micro pores and large inner surface areas that provides an ideal environment for cell attachment, InterOss® is chemically and structurally comparable to mineralized human bone. It is available in sterilized granule form and is dedicated for single uses.

InterOss

Description

InterOss® is a natural hydroxyapatite bone grafting material for use in dentistry. Made from a proven multi-step purification process which leaves only a bone composition, it is a highly purified osteoconductive material for bone regeneration.

Having an interconnected network of macro and micro pores and large inner surface areas that provides an ideal environment for cell attachment, InterOss® is chemically and structurally comparable to mineralized human bone. It is available in sterilized granule form and is dedicated for single uses.

Product Specifications

Small Granules

(0.25 – 1.0 mm)
SKU Volume Weight
IOSG025 0.54 cc 0.25 g
IOSG050 1.08 cc 0.50 g
IOSG100 2.16 cc 1.0 g
IOSG200 4.32 cc 2.0 g

Large Granules

(1.0 – 2.0 mm)
SKU Volume Weight
IOSL050 2.0 cc 0.50 g
IOSL100 4.0 cc 1.0 g
IOSL200 8.0 cc 2.0 g

Indications for Use

InterOss® is recommended for:

  • Filling of peri-implant defects in conjunction with products intended for guided bone regeneration (GBR)
  • Filling of periodontal defects in conjunction with products intended for guided tissue regeneration (GTR) and guided bone regeneration (GBR)
  • Reconstruction or augmentation of the alveolar ridge
  • Filling of periodontal defects
  • Filling of defects after root resection, apicectomy, and cystectomy
  • Filling of extraction sockets to enhance preservation of the alveolar ridge
  • Elevation of the maxillary sinus floor

Studies

InterOss® is 100% natural, biocompatible, highly purified, and has a large inner surface area, multi-porosity, and long term stability. It is validated and documented in clinical studies through universities in the US and abroad and case studies through clinicians involving procedures such as horizontal/vertical augmentation, sinus augmentation, and sinus elevation.

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Inquiry

InterOss® is cleared by the FDA and is registered in Europe, Middle East, Asia, and Latin America. If you are a distributor or clinician and have questions about the product, please submit an inquiry below.