Description
InterOss® Syringe 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.
InterOss® Syringe is designed to deliver InterOss® granules more precisely to the intended treatment site without having to use sterile instruments. It is available in sterilized granule form and is dedicated for single uses.
Description
InterOss® Syringe 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.
InterOss® Syringe is designed to deliver InterOss® granules more precisely to the intended treatment site without having to use sterile instruments. It is available in sterilized granule form and is dedicated for single uses.
Product Specifications
Small Granules
(0.25 – 1.0 mm)
| SKU | Volume |
|---|---|
| IOSGS025 | 0.25 cc |
| IOSGS050 | 0.5 cc |
| IOSGS100 | 1.0 cc |
Large Granules
(1.0 – 2.0 mm)
| SKU | Volume |
|---|---|
| IOLGS050 | 0.5 cc |
| IOLGS100 | 1.0 cc |
| IOLGS150 | 1.5 cc |
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® Syringe 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.