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Alcon’s Latest Equipment Breakthrough Technologies, Unity VCS and Unity CS, Receive U.S. FDA 510(k) Clearance

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Alcon announced that its Unity Vitreoretinal Cataract System (VCS) and Unity Cataract System (CS) have received U.S. FDA 510(k) clearance. These systems are the first innovations from Alcon's Unity portfolio, aimed at transforming surgical procedures in ophthalmology. Alcon plans to gather real-world user feedback in the U.S. before a broad commercialization in 2025. The Unity systems are set to replace Alcon's current leading systems and introduce significant workflow efficiencies. Regulatory submissions will continue globally, with a CE Mark expected in early 2025.

Positive
  • Unity VCS and CS received U.S. FDA 510(k) clearance.
  • Plans to gather real-world feedback before 2025 commercialization.
  • Significant workflow efficiencies over existing systems.
  • First innovations from Alcon’s Unity portfolio.
Negative
  • Commercial launch delayed until 2025.
  • Additional regulatory submissions required globally.

Insights

Alcon’s latest FDA 510(k) clearance for the UNITY® Vitreoretinal Cataract System (VCS) and UNITY® Cataract System (CS) holds significant implications for the medical field and stock market investors alike. This clearance paves the way for Alcon to introduce these breakthrough technologies before their broad commercialization in 2025, addressing a substantial market need.

From a medical standpoint, these developments are noteworthy. The combination of technologies in the Unity VCS and CS systems promise to enhance workflow efficiencies dramatically over existing technologies. This is crucial, as the forecasted rise in the number of cataract surgeries—31 million in 2024, increasing to 37 million by 2029—demands cutting-edge solutions to manage high volumes effectively.

Moreover, the real-world feedback process planned by Alcon will ensure that these systems are refined and validated further before a full-scale launch, potentially solidifying Alcon’s market leadership. The integration of new consumables designed to optimize surgeon, staff and patient experiences further implies a holistic approach to eye care advancements.

From a market perspective, Alcon’s FDA 510(k) clearance for its Unity systems positions the company to capitalize on a growing surgical market. The initiative to gather real-world feedback before broad commercialization indicates a strategic approach to ensure product readiness and market fit, potentially minimizing initial launch risks.

The substantial installed base of more than 28,000 Centurion and Constellation devices targeted for upgrade to the Unity platform presents a significant revenue opportunity for Alcon over the next decade. This transition could lead to a steady stream of revenue from upgrades and consumables, enhancing long-term financial stability.

Market competition in the ophthalmology equipment sector is fierce; however, Alcon’s legacy and existing market leadership provide a robust foundation. The introduction of first-to-market technologies will likely reinforce this leading position, potentially attracting new customers while retaining existing ones.

Financially, this announcement bodes well for Alcon’s future growth. The FDA 510(k) clearance represents a significant milestone that can catalyze investor confidence. The anticipated increase in the number of cataract and vitrectomy procedures globally underscores the potential demand for Alcon’s Unity systems.

Considering the impending broad commercialization in 2025, investors should note that initial expenditures on R&D and marketing will be necessary. However, these costs are likely to be outweighed by the potential revenue from system upgrades and consumables, given the existing customer base and growing procedural volumes. The real-world feedback initiative is a strategic move that may reduce post-launch modifications, conserving resources and assuring a smoother market entry.

Alcon’s focus on regulatory submissions in other markets and the expected CE Mark in early 2025 signal its commitment to global expansion, which could further diversify its revenue streams and reduce geographical sales risks.

  • Combined vitreoretinal-cataract system (VCS) and standalone cataract system (CS) are cleared for use in the U.S.
  • New, proprietary technologies designed to deliver transformative surgical innovation
  • Alcon to immediately begin collecting real-world user experience in the U.S. prior to broad commercialization in 2025
  • First innovations to be introduced from Alcon’s cutting-edge Unity portfolio of surgical equipment

Ad Hoc Announcement Pursuant to Art. 53 LR

GENEVA--(BUSINESS WIRE)-- Regulatory News:

Alcon (SIX/NYSE: ALC), the global leader in eye care dedicated to helping people see brilliantly, today announced that UNITY® Vitreoretinal Cataract System (VCS) and UNITY® Cataract System (CS) have received U.S. Food and Drug Administration (FDA) 510(k) clearance. These innovations are the first to be introduced from Alcon’s highly anticipated Unity portfolio.

“At Alcon, we have a long legacy of involving our customers throughout the research and development process to deliver bold innovation in ophthalmology, and we would like to thank those who helped us arrive at today’s milestone,” said Franck Leveiller, Head of Global R&D and Chief Scientific Officer, Alcon. “We are excited to introduce the next generation of equipment solutions and consumables—in cataract and vitreoretinal surgery—and deliver meaningful impact for Eye Care Professionals and patients.”

Unity VCS and Unity CS introduce significant workflow efficiencies over Alcon’s current market-leading systems, CONSTELLATION® Vision System for vitreoretinal procedures and CENTURION® Vision System with ACTIVE SENTRY® for cataract surgery.

“I have been closely involved in the development of Unity VCS and Unity CS; this truly innovative system is a significant upgrade of Alcon’s best-in-class technologies,” said Steve Charles, MD, FACS, FICS, FASRS. “It is a proud moment to be able to celebrate this clearance.”

Worldwide, there will be an estimated 31 million cataract surgeries in 2024, and that number is expected to increase to 37 million by 2029.1 There will be approximately 2.2 million vitrectomy procedures in 2024 across the globe.2 Alcon is the global market leader for cataract and retina procedural packs (consumables used in each surgery).2,3

Today, there are more than 28,000 Centurion and Constellation devices in the market that will be targeted for upgrade to the Unity platform over the next decade. In addition to the system, Unity VCS and Unity CS bring first-to-market technologies and consumables that are designed to drive significant benefits for the surgeon, staff and patients.

Alcon has tested Unity VCS and Unity CS during investigational advisory wet lab sessions with more than 200 highly experienced surgeons from 30+ countries. Now with 510(k) clearance, Alcon will begin a thorough program to secure real-world feedback before commercial launch in 2025. Regulatory submissions will continue later this year in markets across the globe. CE Mark is expected in early 2025.

Unity VCS and Unity CS are the latest innovations from the Alcon Vision Suite—a portfolio of innovative products designed to help Eye Care Professionals increase clinic and OR efficiency, and deliver exceptional patient experiences. The Alcon Vision Suite will continue to grow with cutting-edge Unity products expected to be introduced over the coming years, adding to our market-leading legacy products which will continue to be available and serviceable. Unity VCS and Unity CS will be supported by Alcon’s training, product maintenance and Services teams.

Cautionary Note Regarding Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as: “anticipate,” “intend,” “commitment,” “look forward,” “maintain,” “plan,” “goal,” “seek,” “target,” “assume,” “believe,” “project,” “estimate,” “expect,” “strategy,” “future,” “likely,” “may,” “should,” “will” and similar references to future periods.

Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties and risks that are difficult to predict. Some of these factors are discussed in our filings with the United States Securities and Exchange Commission, including our Form 20-F. Should one or more of these uncertainties or risks materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those anticipated. Therefore, you should not rely on any of these forward-looking statements.

Forward-looking statements in this press release speak only as of the date they are made, and we assume no obligation to update forward-looking statements as a result of new information, future events or otherwise.

About Alcon

Alcon helps people see brilliantly. As the global leader in eye care with a heritage spanning over 75 years, we offer the broadest portfolio of products to enhance sight and improve people’s lives. Our Surgical and Vision Care products touch the lives of more than 260 million people in over 140 countries each year living with conditions like cataracts, glaucoma, retinal diseases and refractive errors. Our more than 25,000 associates are enhancing the quality of life through innovative products, partnerships with Eye Care Professionals and programs that advance access to quality eye care. Learn more at www.alcon.com.

About UNITY VCS and UNITY CS

Indications / Intended Use: The UNITY® VCS (Vitreoretinal Cataract System) console, when used with compatible devices, is indicated for use during anterior segment (i.e. phacoemulsification and removal of cataracts) and posterior segment (i.e. vitreoretinal) ophthalmic surgery. In addition, with the optional laser this system is indicated for photocoagulation (i.e. vitreoretinal and macular pathologies), iridotomy and trabeculoplasty procedures. The UNITY® CS (Cataract System) console, when used with compatible devices, is indicated for use during anterior segment (i.e. phacoemulsification and removal of cataracts) ophthalmic surgery. Refer to the Directions for Use for the accessories/consumables and User Manual for a complete listing of indications, warnings, cautions and notes.

References

  1. Market Scope 2024 IOL Market Report, 2024.
  2. Market Scope 2024 Retinal Surgical Device Market Report, 2024.
  3. Market Scope 2024 Cataract Surgical Equipment Market Report, 2024.

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Investor Relations

Dan Cravens

Allen Trang

+ 41 589 112 110 (Geneva)

+ 1 817 615 2789 (Fort Worth)

investor.relations@alcon.com

Media Relations

Steven Smith

+ 41 589 112 111 (Geneva)

+ 1 817 551 8057 (Fort Worth)

globalmedia.relations@alcon.com

Source: Alcon Inc. Swiss

FAQ

What are Alcon's new systems approved by the FDA?

Alcon's new Unity Vitreoretinal Cataract System (VCS) and Unity Cataract System (CS) have received FDA 510(k) clearance.

When will Alcon's new Unity systems be broadly commercialized?

Alcon plans to broadly commercialize the Unity systems in 2025 after gathering real-world user feedback.

What efficiencies do Alcon's Unity systems introduce?

Alcon's Unity systems introduce significant workflow efficiencies over their current market-leading systems.

What is the expected global market for cataract surgeries?

The global market for cataract surgeries is expected to increase from 31 million in 2024 to 37 million by 2029.

What is Alcon's next step after the FDA approval?

Alcon will begin collecting real-world user feedback and continue regulatory submissions globally, with a CE Mark expected in early 2025.

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