Clinical Experience

Real Life Experience

Patient and Physician Voices

Watch the attached videos to hear what physicians and their patients have to say about the use of RECELL.

Inside the RECELL System

Patient Voices

Inside the RECELL System

Patient Voices

Inside the RECELL System

Revolutionizing Burn Treatment

Case Reports

Skin Regeneration Transformed

RECELL is a revolutionary approach to overcome limitations associated with traditional autografting techniques with proven clinical results.

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Case Study #1

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Case Study 1 Thumbnail

Case Study #1

RECELL System treatment of deep partial-thickness burn reduced donor site requirements by 97% compared to standard autografting.

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Case Study #2

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Case Study 2 Thumbnail

Case Study #2

Significant reduction of donor skin required with the use of RECELL System treatment for deep partial-thickness burn.

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Case Study #3

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Case Study 3 Thumbnail

Case Study #3

Epidermal regeneration observed at one week for deep partial-thickness facial burn using RECELL System treatment

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Case Study #4

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Case Study #4

Definitive closure obtained for full-thickness burn using RECELL System, treatment in combination with 6:1 meshed autograft.

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Important Safety Information

Indications for Use: The RECELL® Autologous Cell Harvesting Device is indicated for the treatment of acute thermal burn wounds in patients 18 years of age and older. The RECELL® device is used by an appropriately-licensed healthcare professional at the patient’s point of care to prepare autologous Regenerative Epidermal Suspension (RES™) for direct application to acute partial-thickness thermal burn wounds or application in combination with meshed autografting for acute full-thickness thermal burn wounds.

Contraindications: RECELL® is contraindicated for: the treatment of wounds clinically diagnosed as infected or with necrotic tissue, 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. 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 full-thickness burn wounds. 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, >320 cm2, 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 articulated joints, in patients with wounds totaling >50% TBSA.

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

Important Safety Information

Indications for Use: The RECELL® Autologous Cell Harvesting Device is indicated for the treatment of acute thermal burn wounds in patients 18 years of age and older. The RECELL® device is used by an appropriately-licensed healthcare professional at the patient’s point of care to prepare autologous Regenerative Epidermal Suspension (RES™) for direct application to acute partial-thickness thermal burn wounds or application in combination with meshed autografting for acute full-thickness thermal burn wounds.

Contraindications: RECELL® is contraindicated for: the treatment of wounds clinically diagnosed as infected or with necrotic tissue, the treatment of...

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