• Flacon Poudre d'os
  • Greffon osseux PHOENIX® issu de têtes fémorales pour chirurgie orthopédique
  • Flacon Poudre d'os
  • Greffon osseux PHOENIX® issu de têtes fémorales pour chirurgie orthopédique

Phoenix ®

Our PHOENIX® bone grafts are derived from tibial plateau cartilage harvested from living donors during arthroplasty.

These osteo-conductive grafts are indicated for cyst filling, peri-implant filling and sinus lift.

Collected in France, these osteo-conductive grafts are characterized by their safety. Collection is organized using flexible, high-performance logistics, developed on a national scale in compliance with good tissue and cell practices.

Discover

The benefits

At TBF, we design our grafting products with a constant focus on quality, safety and clinical performance. Every PHOENIX® bone graft is prepared according to rigorous, scientifically validated processes that comply with the most stringent regulatory requirements.

Osteoconductive effect

Its natural bone framework and the interconnected porosities of human cancellous bone allow good colonization of the patient’s bone cells and vessels for assured osteoconduction.

Unique treatment process

The PHOENIX® process is a specific viral inactivation, delipidation, freeze-drying and radiosterilization treatment offering every possible guarantee of safety.

Confirmed clinical efficacy

With over 200,000 grafts implanted since 1992 and numerous published scientific studies, TBF has confirmed its expertise as France’s leading tissue bank.

References

Flacon Poudre d'os
Cortico-cancellous bone powders
Cortico-cancellous bone powder 0.25 cc bottle DSC025
Cortico-cancellous bone powder 0.5 cc bottle DSC05
Cortico-cancellous bone powder 1 cc bottle DSC10
Cortico-cancellous bone powder 2 cc bottle DSC20
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Fine cortico-cancellous bone powders
Fine cortico-cancellous bone powder 0.25 cc bottle D2025
Fine cortico-cancellous bone powder 0.5 cc bottle D205
Fine cortico-cancellous bone powder 1 cc bottle D210
Fine cortico-cancellous bone powder 2 cc bottle D220
Flacon Poudre d'os
Cancellous bone powders
Cancellous bone powder in 0.5 cc D905
Cancellous bone powder in 1 cc D910
Cancellous bone powder in 2 cc D920
Cancellous bone powder in 2 cc syringe D920+
Cancellous bone powder in 4 cc D940
Greffon osseux PHOENIX® issu de têtes fémorales pour chirurgie orthopédique
Geometric shapes of cancellous bone
15 x 10 x 1.5 mm slat LC15
15 x 10 x 1.5 mm slat DL15
Block 10 x 20 x 20 mm T04
Block 22 x 22 x 32-34 mm (with dome) T16
Sticks 30 x 10 x 10 mm S03
Cancellous bone chips
Small chips bottle – 5 to 7 cc BS02
Chips flask – 5 to 7 cc B02

Download our documents

Types de documents
  • All
  • Commercial documentation
  • Instructions for use
  • Medical prescription

A unique production process

The PHOENIX® process is a secure, controlled industrial process exclusive to TBF. This process is a specific treatment for viral inactivation, delipidation, freeze-drying and radiosterilization, offering every possible guarantee of harmlessness. Production is carried out in ISO6 & ISO7 controlled atmosphere zones.

  1. Decortication

    Cutting and removing cartilage and cortical bone from the femoral head to allow good solvent penetration.

  2. Mechanical and chemical treatments

    Mechanical and chemical treatments: A succession of chemical baths and mechanical processes are used to inactivate viruses and prions, in accordance with DGS instructions in force since January 1, 2012. Post-treatment analyses confirm the integrity of the bone tissue, the almost total absence of residual solvents and a lipid content of less than 1%.

  3. Lyophilization

    In order to dehydrate bone tissue in depth in a reproducible way, guaranteeing long-term preservation of bone tissue characteristics at ambient temperature.

  4. Gamma radiosterilization

    This process, with its narrow sterilization range (maximum 32 kGy), preserves the biological and structural quality of the bone, while enabling effective sterilization to ISO11137 standards.

  5. Final packaging and storage

    Shelf life of 5 years at room temperature.
    Throughout the PHOENIX® process, several control steps are carried out to ensure that each PHOENIX® graft meets TBF requirements before being released.

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Reimbursement obtained for our bone graft and DBM blends
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TBF at the SFCR annual congress – June 2025 edition
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Would you like to find out more about TBF, its products or services? Our team is at your disposal.