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Global Regenerative Trade

Kanfit 3D

Your Additive Manufacturing Partner 

Custom Specific Medical Implant Design & Manufacturing Company  

Kanfit 3D offers the latest in hybrid manufacturing using EOS M 290 — the leading system for tool-free direct manufacturing in titanium (Ti-64) metal.

Kanfit 3D is ISO 13485:2016 and ISO9001:2015 certified.

 

Kanfit 3D is ready to become your collaborative partner to get your products first to market. Kanfit 3D utilizes the latest manufacturing technologies to achieve precision and accuracy in order to meet the top-most international standards. For the design and production of patient-specific medical devices, KANFIT 3D uses only EU certified biocompatible materials and state-of-the-art design and manufacturing technologies. The processes for implants and single-use surgical instrument production are certified by The Standards Institution of Israel (SII) and fully meet the requirements of the ISO 13485 standard for custom-made medical device manufacturing.

why us

INFORMATION

about the product

KANFIT 3D TECHNOLOGY

KANFIT 3D CUSTOM SPECIFIC IMPLANTS

BENEFITS

Highly efficient

Producing minimal waste​ (as opposed to traditional, subtractive manufacturing with up to 90% waste). 

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‘Impossible’ geometries

Create new ‘impossible’ geometries, complex features and fine details.

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Lighter in weight

Design products that are up to 60% lighter in weight.

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Designs into products quickly

Ideal for rapid prototype development.
 
 

QUALITY ASSURANCE TO THE FIELD OF

ADDITIVE MANUFACTURING

Kanfit 3D specializes in Additive Manufacturing of medical and aerospace components, including custom-made implants, made from Ti-64 titanium metal. Kanfit 3D’s Additive Manufacturing (AM) system sets new standards and offers extensive quality management features and expanded monitoring capabilities. 

KANFIT 3D OFFERS

Metal Additive Manufacturing (AM)

Kanfit 3D's EOS M 290 system offers extensive monitoring functions

Hybrid Manufacturing (combining AM and CNC)

3D metal printing is an exciting new technology with some real major advantages

WE CAN PRINT ANY SOLUTION

PATIENT SPECIFIC IMPLANTS

Services

Concept development and engineering services

Product ideation

from prototype to manufacturing

COMPANY EXPERTISE

At Kanfit 3D, we believe that engineering and technology can be used even more effectively in the healthcare arena to benefit individual patients. We are able to bridge the gap between the physician and individually engineered products.

 Every human body is different and unique and, therefore, each patient’s anatomy should be the starting point for the design and engineering of individual implants and prosthetics.
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We are able to bridge the gap between the physician and individually engineered products. As such we provide patient-specific implants to reconstruct parts of the human skeleton.

OUR STRENGHTS

  • Full-service and outsourcing provider for medical implant manufacturing
  • ISO 13485, ISO 9001 registered
  • Traceability, from raw material to final product
  • Highly experienced staff in the medical manufacturing industry
  • VMI based production
  • Long and reliable relationships with our customers

KANFIT 3D PSI

CASES

GUN SHOT WOUND

Cemented Couboid

DISTAL FEMUR TREATED WITH PLATE AND CEMENT

NON UNION

TUMOR OF THE PROXIMAL AND MIDSHAFT OF RT. FEMUR

Tumor resection over guides + cage with plate

GIANT CELL TUMOR

Fourth finger

RECONSTRUCTION OF LT. MAXILLA AFTER TUMOR RESECTION

Bone taken from fibula

TUMOR IN L4

En block resection + cage

RECONSTRUCTION OF MANDIBULA

DISTAL TIBIA

ANKLE ARTHRODESIS AFTER MULTI TRAUMA

DISTAL TIBIA AND ANKLE

3rd revision case distal tibia ankle fusion

Distal Tibia revision case

DISTAL TIBIA AND ANKLE

Cranial Flap

blowout fracture of the orbital

Oral and Maxillofacial Surgery

Full Calcaneus Tarsal replacement RT

GUN SHOT WOUND

CEMENTED CUBOID

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DISTAL FEMUR TREATED WITH PLATE AND CEMENT

NON UNION

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TUMOR OF THE PROXIMAL AND MIDSHAFT OF RT. FEMUR

Tumor resection over guides + cage with plate

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GIANT CELL TUMOR

FOURTH FINGER

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RECONSTRUCTION OF LT. MAXILLA AFTER TUMOR RESECTION

Bone taken from fibula

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TUMOR IN L4

En block resection + cage

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RECONSTRUCTION OF MANDIBULA

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DISTAL TIBIA

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ORBITA

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ANKLE ARTHRODESIS AFTER MULTI TRAUMA

DISTAL TIBIA AND ANKLE

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3rd revision case distal tibia ankle fusion

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DISTAL TIBIA

REVISION CASE

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CRANIAL FLAP

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blowout fracture of the orbita

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ORAL AND MAXILLO-FACIAL SURGERY

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Full Calcaneus Tarsal replacement RT

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Vivostat Logo

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.
Vivostat Processor Product
  • 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®.
Vivostat Processor Product
  • 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
    The Application Kit contains the Spraypen®1 and all other items required to prepare the system for the delivery of the fibrin sealant or PRF® solution. The Spraypen® is a sterile, disposable, hand held device which delivers the fibrin sealant or PRF® solution to the tissue. The revolutionary and patented design offers the surgeon unparalleled freedom in controlling the application unlike any other product on the market today.

 

1Besides the Spraypen®, the Vivostat® system offers different types of applicators, e.g. the Endoscopic Applicator. For a full list of application devices click here

1-2-3 Spray

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

1. Draw blood from the Patient

Fibrin Prep With Blood Inside

At the time of surgery or up to 24 hours before1, citrate (supplied with the kit) is added to the Preparation Unit. 120 ml of the patient’s own blood is then drawn into the same unit.

2. Process the patient’s blood

Vivostat Processor 800

The Preparation Unit is placed in the Processor Unit. At the touch of a button the process starts; after approx. 25 minutes, an autologous fibrin or PRF® solution is ready for use. No thrombin or bovine components are added to the blood at any time.

3. Load the Applicator Unit and spray

Vivostat Display Applicator

The Fibrin or PRF® solution is easily loaded into the Applicator Unit and applied to the surgical site using one of the unique application devices (e.g. the Spraypen). 1This depends on the type of kit being used. Always consult the “Instructions for Use” supplied with the kit to determine the correct preparation.

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

Presentation DVD from Vivostat A/S on Vimeo.