All products in the Linacol Medical product portfolio have been developed as R&D projects and they have been supported by the Scientific and Technological Research Council of Turkey and Small and Medium Enterprises Development and Support Administration of Turkey.

Linacol Medical production facility is certified by UDEM Certification Company with ISO 13485 certificate and all Linacol Medical products are certified by UDEM with CE certification.

OUR MISSION

LINACOL, AS AN R&D FIRM, COMMITTED TO CONTINUOUS RESEARCH AND DEVELOPMENT AS WE APPLY THE LATEST TECHNOLOGIES IN ORDER TO MAKE LIFE EASIER, HAPPIER AND FULL OF HOPE FOR PATIENTS WORLDWIDE THROUGH THE MOST EFFECTIVE APPLICATIONS AND SOLUTIONS.

EVERY NEW AND INNOVATIVE TECHNOLOGY WE DEVELOP IS OUR SIGNATURE OF HOPE AND COMFORT FOR PATIENTS’ LIVES GLOBALLY.

WE PRODUCE INNOVATIVE TECHNOLOGIES IN THE FIELD OF SYNTHETIC BONE GRAFT.

R & D studies in the health sector aim to improve the health and quality of life of the person.

For this purpose, while we are preparing the ground for innovation with our advanced technologies, we increase the efficiency of our products.

PRODUCTION

In our production facility equipped with state-of-the-art equipment at Hacettepe Teknokent, we produce the latest technology products in 1000 Class and 10000 Class clean rooms according to the latest quality standards, improve the quality of life of patients and ensure that patients look to the future with hope.

CureOs production is carried out in clean rooms located in our production facility and all clean rooms are electronically controlled; For all production parameters such as temperature, pressure, air exchange rate and so on, it is monitored and reported in real time for 24 hours.

Linacol Medical production facility is certified with ISO 13485 Certificate and CE Certificate.

QUALITY

Linacol Medical offers professional service, within the framework of national and international standards, with competent personnel, in accordance with customer requirements, corporate conditions and legal requirements, on the basis of the principles of confidentiality, reliability and traceability, by continuously improving the quality targets, in accordance with TS EN ISO 13485 and TC Ministry of Health Medical Device Regulations.

LINACOL has the quality standards;

ISO 13485
93/42 / EEC CE Full Quality Assurance Certificate

DISCOVER A BETTER BONEGRAFT

CureOs® CUBE

BONE GRAFT

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CureOs® BLOCKS

BONE GRAFT

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CureOs® HTO

BONE GRAFT

Click Here

OUR MISSION

OUR VISION

EVERY NEW AND INNOVATIVE TECHNOLOGY WE DEVELOP IS OUR SIGNATURE OF HOPE AND COMFORT FOR PATIENTS’ LIVES GLOBALLY.

R & D studies in the health sector aim to improve the health and quality of life of the person.

For this purpose, while we are preparing the ground for innovation with our advanced technologies, we increase the efficiency of our products.

PRODUCTION

QUALITY

DISCOVER A BETTER BONEGRAFT

CureOs® CUBE

CureOs® BLOCKS

CureOs® HTO

Quick links

FOLLOW US

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.

OUR MISSION

OUR VISION

EVERY NEW AND INNOVATIVE TECHNOLOGY WE DEVELOP IS OUR SIGNATURE OF HOPE AND COMFORT FOR PATIENTS’ LIVES GLOBALLY.

R & D studies in the health sector aim to improve the health and quality of life of the person.

For this purpose, while we are preparing the ground for innovation with our advanced technologies, we increase the efficiency of our products.

PRODUCTION

QUALITY

DISCOVER A BETTER BONEGRAFT

CureOs® CUBE

CureOs® BLOCKS

CureOs® HTO

Quick links

FOLLOW US

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^®