CAPTURE THE FLOW OF

OSTEOINDUCTIVE POTENTIAL

Influx is a natural bone graft material that provides osteoinductivity and promotes cell ingrowth

why us

Fast growing company

Engaged in developing

Innovative solutions

INFORMATION

about the product

ADVANCED ALLOGRAFT TECHNOLOGY

100% Human Bone

No extraneous carries, fillers or binding agents

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Advanced Processing

Enhanced regenerative capacity and handling compared to particulate DBM.

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Terminally Sterilized

Provides device level assurance of safety ( 10 -6 )

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Osteoinductive

Proven regenerative capacity by exhibiting all five elements of new bone formation in a validated animal modelvolumes (3-10 mL per cycle)

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Osteoconductive

Three dimensional scaffold providing an optimal environment for cellular attachment and proliferation.

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Room Temp Storage

Ambient storage for convenient distribution and consignment.

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Multiple Sizes And Configurations

Cortical Fibers, Strips and DBM Putty available in multiple sizes.

MULTIPLE SIZES AND CONFIGURATIONS FOR EASE-OF-USE

IN A VARIETY OF APPLICATIONS

Influx™ Demineralized Cortical Bone Fibers

An advanced allograft that combines the regenerative capacity of interconnected fibers with the availability of growth factors endogenous to cortical bone.

Proprietary Processing

Proven regenerative capacity in a validated animal model.2
Increased patient safety through terminal sterilization

Novel Small Diameter Fibers

An ideal scaffold for autologous cells to augment conductive and inductive properties.3
Cohesive handling characteristics to provide precise graft placement that is resistant to irrigation.2
Handles best when hydrated with blood, BMA, or PRP.

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Influx™ Demineralized Bone Matrix Putty

Fully moldable, 100% demineralized bone graft putty offers optimal regenerative capacity through a proprietary processing of demineralized cortical fibers and demineralized cortical particulate.

Optimal Regenerative Capacity

Validated to produce a positive osteoinductive response2
Processed for enhanced regenerative capacity compared to particulate DBM1

Ease-of-Use in a Variety of Applications

Maintains moldable, cohesive handling characteristics to fill irregular defects and provide lavage resistance.
Ready-to-use directly out of packaging with no need for graft preparation or hydration.

Download brochure

CAPTURE THE FLOW OF

OSTEOINDUCTIVE POTENTIAL

why us

Fast growing company

Engaged in developing

Innovative solutions

INFORMATION

ADVANCED ALLOGRAFT TECHNOLOGY

100% Human Bone

No extraneous carries, fillers or binding agents

________________________________________________

Advanced Processing

Enhanced regenerative capacity and handling compared to particulate DBM.

________________________________________________

Terminally Sterilized

________________________________________________

Osteoinductive

Proven regenerative capacity by exhibiting all five elements of new bone formation in a validated animal modelvolumes (3-10 mL per cycle)

________________________________________________

Osteoconductive

Three dimensional scaffold providing an optimal environment for cellular attachment and proliferation.

________________________________________________

Room Temp Storage

Ambient storage for convenient distribution and consignment.

________________________________________________

Multiple Sizes And Configurations

MULTIPLE SIZES AND CONFIGURATIONS FOR EASE-OF-USE

IN A VARIETY OF APPLICATIONS

Influx™ Demineralized Cortical Bone Fibers

Influx™ Demineralized Bone Matrix Putty

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THE VIVOSTAT® SYSTEM

The uniqueness of the Vivostat® system is a novel patented biotechnological process that enables reliable and reproducible preparation of autologous Fibrin Sealant or Platelet Rich Fibrin (PRF®) without using cryoprecipitation and without the need for a separate thrombin component.

THE FULLY AUTOMATED VIVOSTAT® SYSTEM CONSISTS OF THREE COMPONENTS:

The Processor Unit is a non-sterile, reusable, fully automated device that controls the biochemical process.

The Processor Unit is used to process the patient’s blood and prepare the Vivostat® Fibrin Sealant or Vivostat PRF® solution.

The Processor Unit is operated by a single button and a display keeps the nurse informed of the remaining process time and status at all times. No specific installation is required and the large wheelbase makes moving it easy.

The Processor Unit can be located in any room or corridor in the operating department. It is most often placed centrally between the operating theatres. This way one Processor Unit can supply a number of operating theatres.

In approx. 25 min a concentrated fibrin sealant or PRF® solution is prepared from the patient’s whole blood.

The Applicator Unit is a non-sterile, reusable, fully automated device that controls the delivery of the Vivostat® Fibrin Sealant or Vivostat PRF®.

The large display and integrated microprocessor automatically primes the Spraypen® and informs the surgeon of the remaining volume of fibrin sealant/PRF® throughout the entire process.

Different spray modes can be selected depending on the actual procedure or area to be covered. Like the Processor Unit it has a large wheelbase and can easily be moved if required.

The disposable set comprises of two parts: A Preparation Kit used to prepare the fibrin sealant or PRF® solution before surgery, and an Application Kit used to activate and apply the fibrin sealant/PRF® solution.

Preparation Kit

The Preparation Kit contains the specially designed Preparation Unit – a sterile disposable device in which the patient’s blood is collected, the biochemical process carried out, and the fibrin sealant or PRF® solution harvested.

The Application Kit

1-2-3 Spray

Three easy steps to prepare Vivostat® Fibrin Sealant or Vivostat PRF®

1. Draw blood from the Patient

2. Process the patient’s blood

3. Load the Applicator Unit and spray

PREPARATION AND APPLICATION

The following video illustrates how to prepare and apply autologous fibrin sealant.

The uniqueness of the Vivostat^® system is a novel patented biotechnological process that enables reliable and reproducible preparation of autologous Fibrin Sealant or Platelet Rich Fibrin (PRF^®) without using cryoprecipitation and without the need for a separate thrombin component.

THE FULLY AUTOMATED VIVOSTAT^® SYSTEM CONSISTS OF THREE COMPONENTS:

The Processor Unit is used to process the patient’s blood and prepare the Vivostat^® Fibrin Sealant or Vivostat PRF^® solution.

In approx. 25 min a concentrated fibrin sealant or PRF^® solution is prepared from the patient’s whole blood.

The Applicator Unit is a non-sterile, reusable, fully automated device that controls the delivery of the Vivostat^® Fibrin Sealant or Vivostat PRF^®.

The large display and integrated microprocessor automatically primes the Spraypen^® and informs the surgeon of the remaining volume of fibrin sealant/PRF^® throughout the entire process.

The disposable set comprises of two parts: A Preparation Kit used to prepare the fibrin sealant or PRF^® solution before surgery, and an Application Kit used to activate and apply the fibrin sealant/PRF^® solution.

The Preparation Kit contains the specially designed Preparation Unit – a sterile disposable device in which the patient’s blood is collected, the biochemical process carried out, and the fibrin sealant or PRF^® solution harvested.

Three easy steps to prepare Vivostat^® Fibrin Sealant or Vivostat PRF^®