Relieving Ocular Pain. Restoring Lives.
At EyeCool, we’re a team of scientists, clinicians, and entrepreneurs united by a singular mission: to bring lasting relief to patients suffering from chronic ocular surface pain—an urgent, overlooked need in eye care.
Ruben Salinas, PhD MBA
President & CEO
Ruben F. Salinas PhD MBA is a serial MedTech entrepreneur and CEO with a track record of founding and scaling companies at the intersection of women’s health, diagnostics, and medical devices. Dr. Salinas previously led Parsagen Diagnostics and AmniSure International to successful exits. He brings over two decades of experience navigating FDA regulatory pathways, clinical trial strategy, and international market entry, with a focus on breakthrough innovations that address unmet medical needs.
Cristos Ifantides, MD MBA
Chief Medical Advisor
Cristos Ifantides, MD, MBA is a fellowship-trained, board-certified anterior segment surgeon who specializes in routine and complex surgeries of the front of the eye. He is a leader in the field and has pioneered new surgical techniques for complex anterior segment surgery that have been adopted across the world. He has published dozens of peer-reviewed articles and has given over 100 invited lectures at local, national, and international conferences.
Prior to entering private practice, Dr. Ifantides was an NIH-funded physician-scientist whose research lab used 3D printing, material science, and drug development to focus on finding solutions to large unmet needs for eye care patients. He is a key opinion leader who has helped lead drug and device companies from concept through commercialization.
Patrick Casey, OD
VP, Clinical Development
Patrick Casey, OD, is a clinical optometrist who transitioned into the ophthalmic MedTech industry over 15 years ago. With a passion for novel technologies that improve quality of life, he thrives in fast-paced startup environments where innovation drives impact. At EyeCool, Dr. Casey is energized by contributing directly to company growth alongside a talented team. Outside of work, he is an avid cyclist who enjoys camping, mountain sports, fishing, and cheering on The Ohio State University football team. Most importantly, he cherishes time spent with his wife and two young daughters.
Joseph Aaron, PMP
Sr. Dir. Product Development
Joe Aaron is a biomedical engineer dedicated to developing medical devices that improve outcomes for both patients and clinicians. His experience spans orthopedics, surgical robotics, anesthesia, emergency medicine, spine care, and ocular devices, with contributions across the design and development of Class I, II, III, and HCT/P devices. Patient safety remains his guiding principle at every stage of product development. In addition to driving product strategy, Joe continues to enjoy hands-on engineering work. Beyond the lab, he spends time with his wife and three young sons, sharing passions for cooking, gardening, volleyball, golf, and 3D printing projects.
Katelyn Li
Director, Product Engineering
Katelyn is a product engineer with a background in biomedical engineering and emphasis on medical device design. A lifelong learner, she is motivated by the constant pursuit of understanding “how things work.” Through her work at EyeCool she strives to advance not only her knowledge of engineering and product development but also of the regulatory, clinical, and economic landscapes in the context of bringing an innovative therapy to market. Outside of the office she enjoys distance running, martial arts, baseball, and exploring the city by bike and foot with her partner. She lives in Cambridge with her partner and two cats.
Palig Mouradian
Sr. Product Engineer
Palig is a Product Engineer with a background in neuroscience and mechanical engineering. She is able to bring in her experience to inform the work she does at EyeCool and contribute to the dynamic work. When not on roller skates she spends time with her pug and black cat.
Gordon Roberts
Regulatory Affairs
Gordon Roberts is an independent consultant who formed his own medical device consulting company in 2012. He has since set up quality management systems, design control and risk management programs for scores of medical device companies. Gordon has over 40 years of experience in Quality Assurance and Regulatory Affairs at large multi-national corporations such as Smith and Nephew, CR Bard and Ion Beam Applications. In addition to creating ISO 13485 and 21 CFR Part 820 and EU MDR compliant quality systems at various start-up operations such as RadioMed and UroMed Corporation.
He has also performed hundreds of quality management system audits and GMP training sessions for both large organizations and start-up companies.