PRESS RELEASE
ALISO VIEJO, Calif., April 13, 2026, OnPoint Vision Inc, a privately held ophthalmic medical device company, announced study expansion of approved Investigational Device Exemption (IDE) begin Phase II of their pivotal clinical trial of the AccuraSee™ Intraocular Pseudophakic Capsular Lens (IOPCL) Magnifier (MAG) for secondary implantation in the capsular bag with a pre-existing 6mm acrylic posterior chamber intraocular lens (IOL). The IOPCL MAG is neutral optic (Plano power) with a central +10.0D 1.8mm zone designed to magnify near images when unilaterally implanted in low vision pseudophakic subjects with inactive Age-Related Macular Degeneration (AMD) at least 6 months after cataract surgery. The IOPCL MAG was originally implanted in First in Human (FIH) study in the US under a separate Early Feasibility Study (EFS) IDE where enrollment and patient follow-up is complete. This EFS IDE study is officially closed.
CAUTION AccuraSee™ IOPCL MAG is an Investigational device. Limited by Federal (or United Sates) law to investigational use.
About the Technology
OnPoint was founded in 2019, the founder and inventor of this technology, Kevin J. Cady, CEO and President has been involved in innovative ophthalmic products for the past 30-years. The IOPCL (Intraocular Pseudophakic Capsular Lens), was originally designed to correct post-cataract residual refractive errors. However, it quickly became apparent that this lens platform could be used for a variety of pseudophakic refractive applications.
