Clinical Development

Patient Outcomes

Clinical Development

Patient Outcomes

Substansive advancements in innovative technology

Patients are the heart of Avita Medical’s Mission

Our objective is to provide healthcare professionals with cutting-edge, regenerative technology to achieve superior outcomes for their patients. Through a series of compelling patient stories, we illustrate the tangible impact and transformative results that our innovative technology brings to patients in need of wound healing and skin restoration. At AVITA Medical, we are dedicated to driving progress, advancing skin restoration, and infusing renewed vitality to the lives we touch.

CASE STUDY 1: DEEP PARTIAL-THICKNESS BURN, FACE
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A 31-year-old female sustained burns with approximately an 11% total body surface area (TBSA) deep partial-thickness burn injury. After prior treatment utilizing a different therapy was unsuccessful, RECELL Spray- On Skin™ Cells were prepared and applied to the wound bed. At post-op day 9, the patient exhibited definitive wound closure and no signs of infection or inflammation. With RECELL alone, the patient experienced progressive re-pigmentation, closely matching the surrounding skin.

CASE STUDY 2: DEEP PARTIAL-THICKNESS BURN, ARM
See Full Case Study 2

A 48-year old male sustained a burn injury. This case study demonstrates treatment of deep partial -thickness burn injuries with the RECELL® System. At 16 weeks, scar outcomes related to pigmentation and height were close to native skin.

CASE STUDY 3: FULL-THICKNESS SKIN DEFECT TRAUMATIC WOUND, ABDOMEN
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A 45-year-old male sustained a 189 cm2 degloving injury caused by a seat belt during a motor vehicle collision. This case focuses on wound closure of the full-thickness injury to his abdomen. The use of RECELL Spray-On Skin™ Cells in combination with a 2:1 meshed split-thickness skin graft (mSTSG)(site B) successfully treated a full-thickness degloving injury and required less donor skin with comparable outcomes to a 1:1 mSTSG (site A).

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Important Safety Information (UNITED STATES)

Indications for use:

The RECELL Autologous Cell Harvesting Device is indicated for the treatment of thermal burn wounds and full-thickness skin defects. The RECELL Device is used by an appropriately licensed and trained healthcare professional at the patient’s point of care to prepare autologous Spray-On Skin Cells for direct application to acute partial-thickness thermal burn wounds in patients 18 years of age and older, or application in combination with meshed autografting for acute full-thickness thermal burn wounds in pediatric and adult patients and full-thickness skin defects after traumatic avulsion (e.g., degloving) or surgical excision (e.g., necrotizing soft tissue infection) or resection (e.g., skin cancer) in patients 15 years of age and older.

CONTRADICTIONS:

RECELL is contraindicated for the treatment of wounds clinically diagnosed as infected or with necrotic tissue present in the wound bed. RECELL is contraindicated for: the treatment of patients with a known hypersensitivity to trypsin or compound sodium lactate (Hartmann’s) solution, patients having a known hypersensitivity to anesthetics, adrenaline/epinephrine, povidone-iodine, or chlorhexidine solutions.

WARNINGS:

Autologous use only. Control infections on wounds prior to application of the cell suspension. Excise the necrotic tissues on wound bed prior to application of the cell suspension. Wound beds treated with a cytotoxic agent (e.g., silver sulfadiazine) should be rinsed prior to application of the cell suspension. RECELL is provided sterile and is intended for single-use. Do not use if packaging is damaged or expired. Choose a donor site with no evidence of cellulitis or infection and process skin immediately. A skin sample should require between 15 and 30 minutes contact with Enzyme. Contact in excess of 60 minutes is not recommended. RECELL Enzyme is animal derived and freedom from infectious agents cannot be guaranteed.

PRECAUTIONS:

RECELL is not intended for use without meshed autograft for treatment of acute full-thickness burn wounds or full-thickness skin defects after traumatic avulsion (e.g., degloving) or surgical excision (e.g., necrotizing soft tissue infection) or resection (e.g., skin cancer). The safety and effectiveness of RECELL without meshed autograft have not been established for treatment of partial-thickness burn wounds: on the hands and articulating joints >320cm2, in patients with wounds totaling >20% total body surface area (TBSA). The safety and effectiveness of RECELL with autografting have not been established for treatment of full-thickness burn wounds: on the hands and articulating joints, and in patients younger than 28 days of age (neonates). The safety and effectiveness of RECELL plus autografting have not been established for application in combination with meshed autografting on full-thickness skin defects after traumatic avulsion (e.g., degloving) or surgical excision (e.g., necrotizing soft tissue infection) or resection (e.g., skin cancer): on the hands and genitalia.

SPECIAL PATIENT POPULATIONS:

The safety and effectiveness of RECELL have not been established for treatment of acute thermal partial-thickness burn wounds in pediatric patients younger than 18 years of age. For complete Important Safety Information, refer to Instructions for Use.

INSTRUCTIONS FOR USE:

Consult the Instructions for Use prior to using RECELL. For complete Important Safety Information, refer to Instructions for Use.

The use of RECELL allows me
to use less donor skin, allows
rapid healing of the interstices
of the meshed graft and spares
my patients from associated
complications related to
delayed wound closure.
– AESTHETIC AND
RECONSTRUCTIVE SURGEON