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AVITA Medical Highlights First U.K. Clinical Experience with RECELL GO at British Burn Association Annual Meeting

(Moderate)
(Positive)
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AVITA Medical (NASDAQ: RCEL) reported first U.K. clinical experience with RECELL GO in 17 burn and reconstructive patients at the 2026 British Burn Association meeting.

According to AVITA Medical, all patients had successful treatment and discharge, with noted workflow benefits, and RECELL GO is CE-marked in Europe/U.K. and authorized in Australia and New Zealand. A separate review of 99 studies in 8,000+ patients found RECELL to be a safe, effective, evidence-based wound management approach.

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Positive

  • First documented U.K. RECELL GO case series in 17 burn patients
  • All patients reportedly discharged without complications after RECELL-based treatment
  • Investigators observed uncomplicated donor-site healing and complete graft take
  • Reported workflow gains: reduced procedural variability and greater operating room efficiency
  • RECELL GO CE-marked in Europe and the U.K.
  • RECELL GO recently authorized in Australia and New Zealand
  • Systematic review: 99 studies and 8,000+ patients support RECELL safety and effectiveness

Negative

  • None.

News Market Reaction – RCEL

+1.78%
+1.78% Session close to close

In the Jun 18 session, RCEL gained 1.78%, reflecting a mild positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement adds early U.K. experience in 17 RECELL GO patients and reinforces RECELL’s backin...
Analysis

This announcement adds early U.K. experience in 17 RECELL GO patients and reinforces RECELL’s backing from 99 studies and over 8,000 patients. Investors may watch for further adoption data and how recent credit facility and warrant terms interact with moderate short positioning.

Key Figures

Case series size: 17 patients Studies in review: 99 studies Patients in review: more than 8,000 patients +3 more
6 metrics
Case series size 17 patients First U.K. clinical experience with RECELL GO
Studies in review 99 studies Systematic review of global RECELL clinical experience
Patients in review more than 8,000 patients Aggregate RECELL experience across included studies
Countries in review 13 countries Geographic breadth of RECELL clinical data
Annual meeting year 2026 British Burn Association Annual Meeting in Nottingham, U.K.
Time span of experience more than two decades Duration of global clinical experience with RECELL

Historical Context

5 past events · Latest: May 17 (Neutral)
5 events
Date Event Sentiment 24h Move Catalyst
May 17 Investor webinar Neutral -8.1% Announcement of investor webinar to review Q1 2026 results and priorities.
May 14 Earnings results Positive +4.6% Q1 2026 results with revenue growth, margin strength, BARDA deal and RECELL GO clearances.
Apr 30 CEO appointment Positive +2.1% Cary Vance named permanent CEO and Jan Stern Reed appointed Board Chair.
Apr 29 Product clearance Positive +2.1% RECELL GO certified by TGA in Australia and listed by Medsafe in New Zealand.
Apr 23 Earnings date set Neutral +3.0% Company scheduled release and call for Q1 2026 financial results.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

ce-marked, autologous cell harvesting, split-thickness skin grafts, systematic review
4 terms
ce-marked regulatory
"RECELL GO is CE-marked in Europe and the U.K. and recently received regulatory authorization"
CE-marked indicates a product meets European Union requirements for safety, performance and legal compliance, allowing it to be sold across the European Economic Area. For investors, a CE mark is like a passport or safety stamp — it reduces regulatory and market-entry risk, can speed sales and adoption across many countries, and signals the maker completed required testing and documentation, which can affect revenue forecasts and valuation.
autologous cell harvesting medical
"“First U.K. Clinical Experience of RECELL GO, an Automated Autologous Cell Harvesting Device"
Autologous cell harvesting is the process of collecting a patient’s own cells for later processing and re‑use in a therapy, like taking seeds from a single garden to replant in the same spot. It matters to investors because using a patient’s own material reduces immune-rejection risk but raises manufacturing complexity, individualized logistics, regulatory hurdles, and per-patient costs, all of which affect scalability, timelines and potential returns.
split-thickness skin grafts medical
"either alone or in conjunction with meshed split-thickness skin grafts"
A split-thickness skin graft is a surgical technique where a thin layer of skin is taken from one part of a patient’s body and transplanted onto a wound or burn to help it heal, like applying a thin patch to cover and close damaged ground. Investors care because the technique drives demand for surgical tools, wound-care products and hospital resources, influences recovery times, reimbursement rates and clinical outcomes, and therefore affects revenue and cost projections in healthcare companies.
systematic review technical
"data presented at the BBA meeting included a systematic review of more than two decades"
A systematic review is a carefully planned and repeatable summary of all available studies on a specific question, using predefined steps to find, evaluate and combine results so conclusions are less biased than a single study. For investors, it matters because it gives a clearer picture of a drug’s safety, effectiveness or market potential—like reading a cookbook that compares every recipe to see which consistently works best—so investment and regulatory judgments rest on stronger evidence.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • First U.K. case series demonstrates successful use of RECELL GO® in 17 burn and reconstructive surgery patients

  • Findings presented at the British Burn Association Annual Meeting support the role of RECELL GO in standardizing preparation of RECELL® Spray-On Skin™ Cells and improving operating room workflow

  • RECELL GO is CE-marked in Europe and the U.K. and recently received regulatory authorization in Australia and New Zealand


VALENCIA, Calif., June 18, 2026 (GLOBE NEWSWIRE) -- AVITA Medical, Inc. (NASDAQ: RCEL, ASX: AVH), a leading therapeutic acute wound care company delivering transformative solutions, today announced the presentation of new clinical data highlighting the first documented use of RECELL GO in the United Kingdom (U.K.) at the 2026 British Burn Association (BBA) Annual Meeting in Nottingham, U.K.

The presentation, titled “First U.K. Clinical Experience of RECELL GO, an Automated Autologous Cell Harvesting Device, in Burn Surgery: A Case Series,” reports outcomes from 17 patients treated at Stoke Mandeville Hospital, one of the U.K.’s leading specialist burn units. Investigators evaluated the use of RECELL GO, AVITA Medical’s next-generation automated system for preparing RECELL Spray-On Skin Cells, across a range of burn and reconstructive procedures. Patients were selected based on injury characteristics and risk factors for healing complications where clinical and aesthetic outcomes are important treatment considerations, including larger and deeper wounds, facial injuries, and patients with higher Fitzpatrick skin types.

“RECELL GO is an important next step in autologous cell harvesting technology,” said Alexandra Atkins-Murray, Consultant Plastic and Burns Surgeon at Stoke Mandeville Hospital and senior author of the study. “Our early experience demonstrates that the automated system integrates seamlessly into clinical practice while maintaining the clinical outcomes we have come to expect from the RECELL manual system. The ability to standardize preparation and free clinical staff during processing offers meaningful advantages for burn centers and surgical teams across the world.”

In the U.K. case series, all patients successfully received RECELL Spray-On Skin Cells prepared using RECELL GO, either alone or in conjunction with meshed split-thickness skin grafts. Investigators reported uncomplicated donor-site healing, complete graft take, and successful patient discharge without complications. The authors also noted workflow benefits, including reduced procedural variability, improved consistency of cell preparation, and greater operating room efficiency.

The investigators concluded that RECELL GO may help expand access to advanced autologous cell therapies by simplifying and standardizing preparation at the point of care, while preserving the clinical benefits associated with RECELL treatment.

“The presentation of this first U.K. clinical experience marks another important milestone in the global adoption of RECELL GO,” said Cary Vance, President and Chief Executive Officer of AVITA Medical. “Clinicians are increasingly recognizing the value of technologies that can reduce donor-site burden, support healing, and improve workflow efficiency. We are encouraged by these early results from the U.K. and look forward to continuing to support burn centers worldwide as RECELL GO expands across Europe, the U.K., Australia, New Zealand, and other international markets.”

The data was presented during the British Burn Association Annual Meeting, one of the leading forums for burn care professionals across the U.K. and Europe. In addition to the RECELL GO case series, data presented at the BBA meeting included a systematic review of more than two decades of global clinical experience with RECELL. The analysis included 99 studies representing more than 8,000 patients across 13 countries and concluded that RECELL is a safe and effective, evidence-based approach to wound management with broad applicability across burn and wound care settings.

About RECELL GO

RECELL GO combines a reusable, AC-powered RECELL Processing Device with a single-use RECELL Preparation Kit to automate and standardize the preparation of RECELL Spray-On Skin Cells at the point of care. The system precisely regulates key processing steps to optimize consistency while reducing operator variability and training burden.

RECELL works by using a small sample of a patient's own healthy skin to prepare a suspension of skin cells that can be sprayed directly onto the wound. This approach can promote healing while reducing the amount of donor skin required compared with traditional grafting techniques.

RECELL GO was CE-marked for commercialization in Europe and the U.K. in 2025 and recently received regulatory authorization in Australia and New Zealand. RECELL technology is also widely used in the United States, where it is FDA approved for the treatment of thermal burn and full-thickness skin defects.

In the U.K. and Ireland, RECELL GO is distributed exclusively by one of the largest independent medical device distributors, Joint Operations Ltd., a specialist provider of advanced wound care and surgical technologies. To learn more visit www.jointoperations.co.uk.

About AVITA Medical, Inc.

AVITA Medical® is a leading therapeutic acute wound care company delivering transformative solutions. Our technologies are designed to optimize wound healing, effectively accelerating the time to patient recovery. At the forefront of our platform is RECELL®, approved by the FDA for the treatment of thermal burn and trauma wounds. RECELL harnesses the healing properties of a patient’s own skin to create Spray-On Skin™ Cells, offering an innovative solution for improved clinical outcomes at the point-of-care. In the U.S., AVITA Medical also holds the exclusive rights to market, sell, and distribute Cohealyx®, an AVITA Medical-branded collagen-based dermal matrix, and the exclusive rights to manufacture, market, sell, and distribute PermeaDerm®, a biosynthetic wound matrix.

In international markets, RECELL is approved to promote skin healing in a wide range of applications, including thermal burn and trauma wounds. RECELL and RECELL GO® are CE-marked in Europe, have TGA certification in Australia, and are listed with Medsafe in New Zealand; RECELL is PMDA-approved in Japan.

To learn more, visit www.avitamedical.com.

CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

This press release may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements are subject to significant risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Forward-looking statements generally may be identified by the use of words such as “anticipate,” “could,” “expect,” “may,” and similar words or expressions, and the use of future dates. Forward-looking statements include, but are not limited to, statements relating to the timing and realization of regulatory approvals of our products; anticipated market share growth and revenue generation; failure to achieve the anticipated benefits from approval of our products; risks associated with international operations and expansion; and other business effects, including the effects of industry, as well as other economic or political conditions outside of the Company’s control. These statements are made as of the date of this press release, and the Company undertakes no obligation to publicly update or revise any of these statements, except as required by law. For additional information and other important factors that may cause actual results to differ materially from forward-looking statements, please see the “Risk Factors” section of the Company’s latest Annual Report on Form 10-K and other publicly available filings for a discussion of these and other risks and uncertainties.

Investor & Media Contact:
Ben Atkins
Phone +1-805 341 1571
investor@avitamedical.com | media@avitamedical.com

Authorized for release by the Chief Financial Officer of AVITA Medical, Inc.

©2026 AVITA Medical. AVITA Medical®, the AVITA Medical logo, Cohealyx®, RECELL®, RECELL GO®, and Spray-On Skin Cells are trademarks of AVITA Medical. PermeaDerm® is a registered trademark owned by Stedical Scientific, Inc. All other trademarks are the properties of their respective owners.


FAQ

What did AVITA Medical (NASDAQ: RCEL) announce about RECELL GO at the 2026 British Burn Association meeting?

AVITA Medical announced first U.K. clinical experience with RECELL GO in burn and reconstructive surgery. According to AVITA Medical, the 17-patient case series showed successful RECELL Spray-On Skin Cells preparation, positive healing outcomes, and operating room workflow benefits at Stoke Mandeville Hospital.

What were the key results from the first U.K. RECELL GO case series in 17 patients?

The 17 patients all successfully received RECELL Spray-On Skin Cells prepared with RECELL GO. According to AVITA Medical, investigators reported uncomplicated donor-site healing, complete graft take, and patient discharge without complications, suggesting RECELL GO can preserve clinical outcomes seen with the manual RECELL system.

How does RECELL GO aim to improve burn surgery workflow for AVITA Medical (RCEL)?

RECELL GO is designed to automate and standardize preparation of RECELL Spray-On Skin Cells. According to AVITA Medical, investigators noted reduced procedural variability, improved consistency of cell preparation, and greater operating room efficiency, while freeing clinical staff during processing in burn and reconstructive procedures.

In which regions is RECELL GO currently authorized or CE-marked for AVITA Medical (RCEL)?

RECELL GO is CE-marked in Europe and the United Kingdom and recently authorized in Australia and New Zealand. According to AVITA Medical, this supports ongoing international expansion of the automated autologous cell harvesting device across burn centers in these key global markets.

What did the systematic review of RECELL clinical experience reveal for AVITA Medical (RCEL)?

The review covered 99 studies representing more than 8,000 patients across 13 countries. According to AVITA Medical, the analysis concluded that RECELL is a safe and effective, evidence-based approach to wound management with broad applicability across burn and wound care settings.

How were patients selected for RECELL GO treatment in the U.K. case series (RCEL)?

Patients were chosen based on injury characteristics and risk factors for healing complications. According to AVITA Medical, selection emphasized larger or deeper wounds, facial injuries, and higher Fitzpatrick skin types, where both clinical and aesthetic outcomes are important treatment considerations in burn and reconstructive surgery.