I-PEN is the world’s first, hand-held in-vivo device for measuring elevated tear film osmolarity levels associated with mild, moderate and severe Dry Eye Disease. The I-PEN, an in-practice dry eye screening device, provides rapid and reliable tear osmolarity levels for patient presenting with dry eye symptoms as well as pre- and post-surgical cases.
• Quantitative measurement – easy to record and follow over time
• Rapid results – less than 5 seconds
• Handheld, light & simple to use
• Affordable point-of-care testing
The I-PEN requires single-Use-Sensors (SUS), sold separately.