
Dear Stakeholders,
I want to take a moment to update you on our progress with the development of Ocumetics’ accommodative intraocular lens (AIOL), which will soon undergo its first-in-human (FIH) trials.
As you know, we are committed to pioneering advanced ophthalmic technologies that will transform the way we treat cataracts and other vision conditions. In recent internal testing of our AIOL, we identified an opportunity to make key design improvements that will enhance both its performance and safety profile. These important improvements do not require significant costs or delays, but they do require adjustments to our current manufacturing process.
To implement these changes, we will need to reorder raw materials, create new lens moulds, and conduct additional internal testing to ensure the lens meets the highest safety, efficacy, and regulatory standards. As a result, we are adjusting our timeline for the first-in-human surgeries. We now anticipate that the FIH trials will begin approximately 6-8 weeks from our previously published date.
I want to emphasize that this decision, though it results in a delay, reflects our unwavering commitment to delivering a product that meets the highest possible standards. Moving a product from concept to human trials is a rigorous process, and it is essential that we maintain the highest level of quality and safety at every stage. These enhancements to the AIOL will improve its overall performance and ensure that we are providing the best possible solution for those impacted by cataracts and other vision challenges.
I am confident that this improvement will result in a more effective, safe, and reliable lens that will set new benchmarks in the ophthalmic industry.
Thank you for your continued support as we strive to bring this transformative technology to market.
Best Regards,
Dean Burns
President & CEO
Ocumetics Technology Corp.
Key Highlights Group Two clinical study underway – Patient recruitment has begun in Mexico City, with surgeries targeted for Fall 2026. Moving beyond safety – The Group Two study will evaluate the Ocumetics Lens for safety plus near-and distance-vision performance. Next-generation technology – Patients will receive the latest-generation Ocumetics Lens implanted with an enhanced delivery system. 12-month data milestone approaching – Group One patients are
Calgary, Alberta – TheNewswire – August 24, 2026 – Ocumetics Technology Corp. (“Ocumetics” or the “Corporation”) (TSXV: OTC) (OTCQB: OTCFF) (FRA: 2QBO) announces that it has completed the third and final tranche of the private placement previously announced by the Corporation on July 7, July 29, July 30, 2026 and July 31, 2026 (the “Offering”). The Corporation
Key Highlights Precision molds received for manufacturing of new optimized accommodating intraocular lenses Production and testing of next-generation lenses now underway New lens design incorporates insights from Group One First-in-Human study Group Two preclinical surgeries targeted for early Q3 2026 FDA Investigational Device Exemption (IDE) preparation advancing Calgary, Canada – TheNewswire – May 12, 2026
Calgary, Alberta – TheNewswire – April 29, 2026 – Ocumetics Technology Corp. (“Ocumetics” or the “Corporation”) (TSXV: OTC) (OTCQB: OTCFF) (FRA: 2QBO) announces that it proposes to complete a private placement (the “Offering”) of up to 2,800,000 units of the Corporation (“Units”) at a price of $0.55 per Unit for gross proceeds of up to


