What is ForeseeHome AMD Home Monitoring Program®?
ForeseeHome is the first FDA-cleared, home-based monitoring device for patients with dry age-related macular degeneration (AMD).
ForeseeHome is intended for use in the detection and characterization of central and paracentral metamorphopsia (visual distortion) in patients with age-related macular degeneration, as an aid in monitoring progression of disease factors causing metamorphopsia including but not limited to choroidal neovascularization (CNV). It is intended to be used at home for patients with stable fixation.
Important Risk Information
ForeseeHome is for prescription use only and is intended to be used in addition to regular eye exams. ForeseeHome is a diagnostic test and does not diagnose any disease or condition; ForeseeHome diagnostic test results are provided to your eye doctor. Diagnosis is performed by your doctor. It is possible for your eye disease to progress while using ForeseeHome therefore it is important to keep your regularly scheduled eye exams.
ForeseeHome is not appropriate for all patients. If you cannot use a computer mouse or have other eye conditions, ForeseeHome may not be right for you. In this case, talk to your eye doctor about other at-home monitoring options to protect your vision.
To report a product complaint related to ForeseeHome, please email firstname.lastname@example.org. You can also report a product complaint to the FDA directly www.fda.gov/medwatch. More information on reporting product complaints to the FDA can be found here.