InterOss® Syringe Cancellous Bone Graft (0.25-1.0mm)) 0.25cc

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InterOss® Syringe Cancellous Bone Graft (0.25-1.0mm)) 0.25cc
Item Number: IOSGS025

InterOss® Syringe Cancellous Bone Graft (0.25-1.0mm)) 0.25cc

InterOss® Syringe Anorganic Cancellous Bone Graft

100% Natural, Biocompatible, Highly Purified, Large Inner Surface Area, Long Term Stability, Multi-Porosity


InterOss® Syringe  like applicator was designed to deliver InterOss® granules more precisely to the intended treatment site without having to use other sterile instruments. The InterOss® granules can be wetted with either the patient’s blood or sterile physiological saline solution by pulling back and then pressing down on the plunger. A removable filter cap prevents granules from falling out of the syringe-like applicator during storage and wetting.

Contains bone grafting material composed of hydroxyapatite (HAp) and derived from Australia bovine bone (BSE free).

The highly purified osteoconductive material comes in an easy to use prefilled syringe. Due to its natural origin, InterOss® Syringe granules are chemically and structurally comparable to mineralized human bone (nanocrystalline natural apatite). The InterOss® Syringe is supplied sterile and is dedicated for single-use.

The presence of a macroporous structure favors cell ingrowth, while the micropores allow the penetration of body fluids into the implant. The microporosity can also be used to manipulate resorption and dissolution rate: the greater the microporosity, the greater the degradation rate.

The pore structure and interconnected pore system of InterOss® allows the grafting material to act as a guide for body fluids, growth factors, blood vessel, bone marrow, and bone cells.



Mesopore (10 – 100μm)

Macropore (>100μm)

Micropore (<10μm)

Anorganic Bovine Bone Substitute

Bovine Origin
Highly Purified
Large Inner Surface Area
Long-Term Stability

  • Storage: InterOss® should be stored in a dry, clean and well ventilated place at ambient temperature (15-25°C/59-77°F). Keep the product in aseptic conditions until use.
  • Sterilization: InterOss® is sterilized using gamma irradiation. Appropriate aseptic technique should be observed in all operations. The package should be inspected prior to use to ensure that the sterile barrier has not been compromised.
  • Caution: Federal (USA) law restricts this device to sale by or on the order of a licensed dentist.
  • InterOss®  is certified under FDA, CE, KFDA regulations