The secret ingredient to healing? Your patient.

Aurix® is a breakthrough wound care solution that starts and ends with the patient. A biodynamic hematogel that harnesses a patient's innate healing mechanisms to jumpstart the natural repair process.

  • Visible Results in Days, Not Weeks
  • Broad treatment flexibility across patient profiles
  • 5-8 minute point-of-care preparation
Schedule 15 Minute Virtual Product Overview

Safe, Rapid and Effective Point-of-Care Preparation

Aurix gel is derived from a patient's own platelets and plasma. Once applied, Aurix goes to work stimulating the body's natural ability to form new tissue, fill in wound defects and reduce wound volume.

What is Aurix Diagram How it works overview

Treatment Process

The Aurix System is used at point-of-care for the safe and rapid preparation of biodynamic hematogel from a small sample of a patient's own blood. Product preparation and application can be completed in less than 10 minutes using four rapid and easy steps.

Step 1

Draw It

Take a small amount of the patient's blood.

Step 2

Spin It

Use the Aurix System centrifuge to separate the platelets (1 minute spin).

Step 3

Mix It

Mix with additives supplied by the Aurix Reagent Kit to produce a golden biodynamic gel.

Step 4

Apply It

Apply over the entire wound, starting with tunnels and undermining, and cover with a clear dressing.

Demonstrated Clinical Efficacy

Aurix has a 96.5% positive response rate in all types of chronic wounds. It is the only therapy of its kind that is FDA-cleared for use on ulcers and wounds of all types.

96.5%
Response rate in less than 15 days with an average of 2.8 treatments.
81.3%
Healed in standard size Diabetic Foot Ulcers vs 42.1% in control group.
6
Weeks mean time to full healing for DFUs. Healing seen in wounds >337 days old.

FDA Clearance & Indications

The Aurix System is the only platelet-based system to produce a proprietary biodynamic gel formulation that is FDA-cleared for wound management. Suitable for exuding wounds and management of mechanically and surgically debrided wounds.

  • Stalled or difficult-to-manage wounds
  • Full or partial thickness wounds
  • Exposed bone or tendon
  • Undermining, sinus tracks, or tunnels
  • Diabetic ulcers
  • Venous ulcers
  • Stage IV pressure injuries

Frequently Asked Questions

Can Aurix be stored for later use?
Once formulated from the patient's blood, Aurix cannot be stored for use at a later time. It is a living tissue and must be made fresh at the time of wound application.
Where does the Aurix process take place?
The centrifuge and kit were designed to be small and portable so that the processing of Aurix can occur in minimal space, such as at the bedside, or in the patient treatment room. It may be used safely in inpatient, outpatient, and long-term care settings.
How much blood is drawn?
Blood draw volumes are adjusted to accommodate wounds of varying size. The flexibility afforded by the Aurix System allows a minimal amount of blood to be drawn in increments of 5 mL. A routine blood draw of 20 mL typically produces 8 mL of platelet/plasma fraction.
Can Aurix be used on exposed bone and tendon?
Yes, as long as the area has been debrided of most of the nonviable or necrotic tissue. Data from clinical case studies indicates granulation tissue growth over exposed bone and tendon during the wound repair process.