ESSILOR® STELLEST® 2.0 LENSES
Made to help your child see clearly while helping manage myopia for tomorrow, the new Essilor® Stellest® 2.0 lenses are designed for children as young as 6 years old to correct myopia and help slow its progression.
The next generationof lenses.Twice the power. 1
In 2020, Essilor® unveiled the first generation of Essilor® Stellest® lenses, slowing myopia progression by 67% on average, helping millions of children worldwide.
Building on the success of the previous generation, Essilor® Stellest® 2.0 lenses provide twice the power, slowing eye growth by 1.88 times more than with the previous generation.
Manage myopiaprogression via H.A.L.T.MAX technology (9)
Essilor® Stellest® 2.0 lenses provide twice the signal for slowing myopia progression10, delivering significantly better results11 12 vs the first generation of Essilor® Stellest® lenses. The enhanced efficacy of Essilor® Stellest® 2.0 lenses is supported by clinical trial results13.
• Correct myopia
Designed to provide sharp vision with your child’s prescription
• Myopia management
Slow myopic eye growth with H.A.L.T. MAX technology
wondering if Essilor® Stellest® 2.0 is right for your child?
Talk with an IRIS eye care professional to learn more about this innovative myopia management solution.
1.The mention "twice the power" refers to a depth of unfocused light volume (by design) twice (or more) greater than that of Essilor® Stellest® lenses,— and is not associated with a doubling of lens power, microlens power or efficiency.
2.Based on the 12-month results of a prospective, randomized, double-blind, contralateral crossover clinical trial conducted in Singapore on 50 children.
3.Raveendran RN, et al. Effect of increased power and asphericity of highly aspherical lenslets on myopia control efficacy: a contralateral crossover study. Transl Vis Sci Technol. 2025;14(11):9.
4.No significant difference in distance BCVA between Essilor® Stellest® and Essilor® Stellest® 2.0 lenses when looking through the central zone of the lens (Drobe B, et al. Effect of increased power and asphericity of lenslets in myopia control spectacle lenses on short-term visual performance. Invest Ophthalmol Vis Sci. 2025;66:2144)
5.When viewed through the peripheral zone of the aspheric microlenses, no significant difference was observed between Essilor® Stellest® and Essilor® Stellest® 2.0 lenses for high-contrast, low-contrast, and low-contrast near visual acuity (VA). (EssilorLuxottica. Internal data. 2025 Impact of increased microlens power and asphericity on the short-term visual performance of myopia control lenses.)
6.Essilor® Stellest® 2.0 lenses are made of AIRWEAR® polycarbonate which offers impact resistance and blocks 100% of UV transmission.
7.Based on the 12-month results of a prospective, randomized, double-blind, contralateral crossover clinical trial conducted in Singapore on 50 children.
8.Raveendran RN, et al. Effect of increased power and asphericity of highly aspherical lenslets on myopia control efficacy: a contralateral crossover study. Transl Vis Sci Technol. 2025;14(11):9.
9.HALT stands for Highly Aspherical Lenslet Target and does not mean that the progression of myopia is "stopped" or "blocked".
10.The mention "twice the power" refers to a depth of unfocused light volume (by design) twice (or more) greater than that of Essilor® Stellest® lenses, and is not associated with a doubling of lens power, microlens power or efficiency.
11.Based on the 12-month results of a prospective, randomized, double-blind, contralateral crossover clinical trial conducted in Singapore on 50 children.
12.Raveendran RN, et al. Effect of increased power and asphericity of highly aspherical lenslets on myopia control efficacy: a contralateral crossover study. Transl Vis Sci Technol. 2025;14(11):9.
13.Raveendran RN, et al. Effect of increased power and asphericity of highly aspherical lenslets on myopia control efficacy: a contralateral crossover study. Transl Vis Sci Technol. 2025;14(11):9.
*Essilor® Stellest® lenses are not currently available in all countries, including the United States, and have not been authorized by the US FDA.