Vericel Corporation to Present at 2026 Truist Securities MedTech Conference
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jun 09 2026
0mins
Source: Newsfilter
- Conference Presentation: Vericel Corporation is set to present at the Truist Securities MedTech Conference on June 16, 2026, showcasing its advanced therapies in sports medicine and severe burn care, which is expected to attract attention from investors and industry experts, thereby enhancing the company's visibility in the medical technology sector.
- Product Portfolio Overview: The company markets three primary products in the U.S., including MACI® for knee cartilage repair, Epicel® for patients with deep burns, and NexoBrid® for eschar removal, highlighting Vericel's leadership in the biotechnology field with these innovative offerings.
- Market Positioning: Vericel focuses on the sports medicine and severe burn care markets, combining innovations in biology with medical technologies to create a highly differentiated portfolio of cell therapies and biologics, aimed at meeting the growing patient demand and improving treatment outcomes.
- Investor Relations: The company will provide a webcast of the presentation on its Investor Relations section, further enhancing communication with investors and showcasing its ongoing innovations and market potential in the medical technology arena.
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Analyst Views on VCEL
Wall Street analysts forecast VCEL stock price to rise
5 Analyst Rating
4 Buy
1 Hold
0 Sell
Strong Buy
Current: 39.130
Low
55.00
Averages
57.67
High
60.00
Current: 39.130
Low
55.00
Averages
57.67
High
60.00
About VCEL
Vericel Corporation is a provider of advanced therapies for sports medicine and severe burn care markets. It has a differentiated portfolio of cell therapy and specialty biologic products. It markets three products in the United States. MACI (autologous cultured chondrocytes on porcine collagen membrane) is an autologous-cellularized scaffold product indicated for the repair of symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults. Epicel (cultured epidermal autografts) is a permanent skin replacement for the treatment of patients with deep dermal or full thickness burns greater than or equal to 30% of total body surface area. The Company also holds a license for North American rights to NexoBrid (anacaulase-bcdb), a biological orphan product containing proteolytic enzymes, which is indicated for eschar removal in adults and pediatric patients with deep partial-thickness and/or full-thickness thermal burns.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Scientific Shift: The field is transitioning from traditional tissue replacement to regeneration, utilizing biomaterials and cell therapies to help the body heal itself, thereby enhancing treatment outcomes and improving patient quality of life.
- Demographic Demand Drivers: The aging population and the rise of chronic diseases like diabetes are increasing the need for tissue repair, particularly in trauma and reconstructive surgery, which is driving market demand for regenerative solutions.
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- Conference Presentation: Vericel Corporation is set to present at the Truist Securities MedTech Conference on June 16, 2026, showcasing its advanced therapies in sports medicine and severe burn care, which is expected to attract attention from investors and industry experts, thereby enhancing the company's visibility in the medical technology sector.
- Product Portfolio Overview: The company markets three primary products in the U.S., including MACI® for knee cartilage repair, Epicel® for patients with deep burns, and NexoBrid® for eschar removal, highlighting Vericel's leadership in the biotechnology field with these innovative offerings.
- Market Positioning: Vericel focuses on the sports medicine and severe burn care markets, combining innovations in biology with medical technologies to create a highly differentiated portfolio of cell therapies and biologics, aimed at meeting the growing patient demand and improving treatment outcomes.
- Investor Relations: The company will provide a webcast of the presentation on its Investor Relations section, further enhancing communication with investors and showcasing its ongoing innovations and market potential in the medical technology arena.
See More
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- Strong Financial Performance: Vericel's Q2 revenue climbed 20% year-over-year to $63.2 million, driven by a 21% increase in its MACI cartilage repair therapy, while gross margin improved to 74%.
- Future Growth Potential: The company received FDA clearance for a Phase 3 study of MACI for ankle cartilage defects, broadening its growth avenues, and management expresses confidence in continued revenue growth and profitability.
See More
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- Market Size Forecast: Independent estimates indicate that the regenerative medicine market will reach tens of billions of dollars by 2026, with projections to exceed $100 billion within a decade, reflecting a compound annual growth rate often estimated in the high teens to mid-20s percent, showcasing rapid growth potential in the sector.
- Scientific Shift: The field is transitioning from traditional tissue replacement to regeneration, utilizing biomaterials, cell therapies, and 3D bioprinting technologies aimed at enabling the body to heal itself, thereby enhancing treatment outcomes and patient quality of life.
- Demographic Drivers: The aging population, diabetes epidemic, and increasing incidence of chronic non-healing wounds are driving demand for regenerative solutions, particularly in aesthetics and reconstructive surgery, leading to a diversified market need.
- Industry Complexity: The regenerative medicine sector faces multiple challenges including reimbursement policies, regulatory pathways, and manufacturing scale, as evidenced by recent upheaval in the U.S. skin substitute market, highlighting the significant impact of payer policies on company profitability and the need for adaptability in response to market changes.
See More
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- Market Growth: The regenerative medicine market is projected to reach tens of billions of dollars by 2026, with forecasts suggesting it could exceed $100 billion within a decade, reflecting a compound annual growth rate often estimated in the high teens to mid-20s percent range, indicating substantial commercial potential.
- Scientific Shift: The field is transitioning from traditional tissue replacement to regeneration, utilizing biomaterials and cell therapies to help the body heal itself, thereby enhancing treatment outcomes and improving patient quality of life.
- Demographic Demand Drivers: The aging population and the rise of chronic diseases like diabetes are increasing the need for tissue repair, particularly in trauma and reconstructive surgery, which is driving market demand for regenerative solutions.
- Policy and Market Complexity: Despite the promising market outlook, changes in policy and regulatory pathways are crucial for company success, as evidenced by recent upheaval in the U.S. skin substitute market, highlighting the significant impact of reimbursement policies on revenue.
See More
Conexeu Sciences Advances Wound Care Technology
- Manufacturing Scale-Up: On June 8, 2026, Conexeu Sciences announced significant progress in scaling up manufacturing for its lead wound care device, with plans to submit a 510(k) application to the FDA in Q1 2027, indicating a critical transition from lab research to manufacturing and regulatory testing, which underscores the maturity and market potential of its technology.
- Platform Technology Advantage: The company's CXU™ platform is a proprietary extracellular matrix designed to rapidly transition into a stable gel scaffold at body temperature, effectively filling complex wound geometries, which is expected to significantly enhance wound care outcomes and meet the market demand for efficient regenerative materials.
- Broad Market Potential: The wound care device market was valued at approximately $2.6 billion in 2023 and is projected to approach $4.2 billion by 2033; Conexeu's technology is not limited to wound care but also plans to expand into aesthetics and regenerative medicine, showcasing its commercialization diversity and potential.
- Intense Industry Competition: While Conexeu's prospects in regenerative medicine are optimistic, it faces competition from established companies like Organogenesis, which have built strong brands and customer bases in the market, necessitating continuous innovation in technology and market strategy for Conexeu to stand out.
See More
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- Manufacturing Scale-Up: On June 8, 2026, Conexeu Sciences announced significant progress in scaling up manufacturing for its lead wound care device, with plans to submit a 510(k) application to the FDA in Q1 2027, indicating a critical transition from lab research to manufacturing and regulatory testing, showcasing the technology's maturity and market potential.
- Platform Technology Advantage: The company's CXU™ platform utilizes a thermosensitive extracellular matrix that rapidly transitions to a stable gel scaffold at body temperature, designed to fill complex wound geometries better than traditional materials, which is expected to drive its broad application in wound care and aesthetics markets.
- Significant Market Potential: The wound care devices market was valued at approximately $2.6 billion in 2023 and is projected to approach $4.2 billion by 2033, with Conexeu's technology poised to capture a share in this rapidly growing market driven by aging populations and increasing chronic wounds.
- Intense Competitive Landscape: Despite the promising outlook for Conexeu in regenerative medicine, it faces fierce competition from established players like Organogenesis and Integra, which have built strong brands and product lines in the market, necessitating Conexeu to overcome substantial regulatory and financing challenges to achieve commercialization.
See More
Vericel Corporation to Present at 2026 Truist Securities MedTech Conference
- Conference Presentation: Vericel Corporation is set to present at the Truist Securities MedTech Conference on June 16, 2026, showcasing its advanced therapies in sports medicine and severe burn care, which is expected to attract attention from investors and industry experts, thereby enhancing the company's visibility in the medical technology sector.
- Product Portfolio Overview: The company markets three primary products in the U.S., including MACI® for knee cartilage repair, Epicel® for patients with deep burns, and NexoBrid® for eschar removal, highlighting Vericel's leadership in the biotechnology field with these innovative offerings.
- Market Positioning: Vericel focuses on the sports medicine and severe burn care markets, combining innovations in biology with medical technologies to create a highly differentiated portfolio of cell therapies and biologics, aimed at meeting the growing patient demand and improving treatment outcomes.
- Investor Relations: The company will provide a webcast of the presentation on its Investor Relations section, further enhancing communication with investors and showcasing its ongoing innovations and market potential in the medical technology arena.
See More
Soleus Capital Increases Stake in Vericel
- Share Increase: Soleus Capital added 1,785,079 shares of Vericel in Q1, with an estimated trade value of $63.40 million, indicating strong confidence in the company's prospects.
- Stake Value Growth: By quarter-end, Vericel's total stake value reached $82.00 million, an increase of $54.49 million from the previous quarter, reflecting positive impacts from both trading and stock price movements.
- Strong Financial Performance: Vericel's Q2 revenue climbed 20% year-over-year to $63.2 million, driven by a 21% increase in its MACI cartilage repair therapy, while gross margin improved to 74%.
- Future Growth Potential: The company received FDA clearance for a Phase 3 study of MACI for ankle cartilage defects, broadening its growth avenues, and management expresses confidence in continued revenue growth and profitability.
See More
