Inspire is currently only available in the US

IrisVision Smart Glasses for Retinitis Pigmentosa

IrisVision-a class-1 registered medical device that leverages technology to help visually impaired and low-vision to regain their vision and reclaim their independence.

Get a Free Consultation

Start Your 30 day risk-free trial today. Terms and conditions apply

Adopt A Positive Outlook On Life

  • Regain Leftover Vision
  • Restores sight by using your leftover vision to reclaim your independence.
  • Stay Connected & Entertained:
  • Unlimited access to entertainment, social media and more.
  • 100% Remote Support
  • Remote screening delivery. 1-on-1 training etc.

Thousands of low vision and vision impaired individuals across the global have experienced the change.

Are you ready?

Awards Honorary Mentions & Impact

“Did you know IrisVision was Awarded The World Changing Idea for 2020?”

IrisVision received the Fast Company Honoree Award for The World Changing Idea for 2020.

The World Changing Ideas program focuses on honoring companies seeking to elevate products and brave concepts that make the world better.

World Class Partnership

World Class Partnership

Types Of Retinitis Pigmentosa That Are Supported By IrisVisions

  • Usher Syndrome
  • Leber’s Congenital Amaurosis (LCA)
  • Cone-rod Dystrophy (CDR)
  • Pigmentary Retinopathy
  • CMV Retinitis
  • Bardet-Biedl Syndrome
    And more…

Bringing You Closer To Things You Love

Watch stream and save your favorite YouTube Videos

Capture and save photos of your most treasured memories

Revisit the habit of reading with ease using optical character recognition (OCR)

Benefit your very own personal assistant with smart voice commands feature

Round-the-clock Remote Customer Support

Our team helps you get started and make the most out of the wearable low vision solution, available for you round-the-clock.

Our esteemed panel of expert coaches help you better understand and easily adapt to the IrisVision headset through 1-on-1 coaching sessions done remotely.

Uninterrupted Cellular Connectivity

IrisVision Live features rely on cellular or WiFi connectivity. Enjoy up to 500MB of data usage until your device has been set up on your Wi-Fi network within 60 days from shipment. For those without access to Wi-Fi, IrisVision now offers an extended Data Usage Plan. For $20 a month* use up to 500MB of data to stream and save Youtube videos, use Amazon Alexa smart commands and much more.

Join us for a 30-day trial period

Step 1

Fill and submit the form

Step 2

Receive free consultation to assess and monitor the feasibility of lrisVision by one of our specialists

Step 3

Upon meeting the eligibility criteria you can avail a 30 free trial

Step 4

Our expert coaches will then provide 1-on-1 free training for you to make the most of IV Live

Step 5

In case if the IV Live experience is not for you, the device can be returned

Step 1

Fill and submit the form

Step 2

Receive free consultation to assess and monitor the feasibility of lrisVision by one of our specialists

Step 3

Upon meeting the eligibility criteria you can avail a 30 free trial

Step 4

Our expert coaches will then provide 1-on-1 free training for you to make the most of IV Live

Step 5

In case if the IV Live experience is not for you, the device can be returned

“It was not what I had expected – nothing is like the IrisVision. IrisVision is incredible! Just a few days ago I replaced three electrical outlets without any problems. IrisVision is wha’s keeping me employed!”

Ed Combis, A former Special Weapons Technician with Retinitis Pigmentosa

Retinitis Pigmentosa FAQ's

As indicated that RP cannot be completely cured, some studies have found that a daily intake of Vitamin A palmitate (15000 IU) decreased the progression of RP in some patients. The Argus retinal prosthesis is a surgical treatment which involves an electronic sub-retinal implant in place of the damaged retina of the patients.

Gene therapy is also a potential treatment being considered for replacing the mutated retinal gene with a healthy gene variant to resume the healthy functioning of photoreceptor cells in the patient of RP but this treatment is still underway.

RP is a chronic condition that cannot be prevented or reversed, however, its progress can be slowed down from further progression by taking preventive measures for management.Helpful low-vision aid devices designed under the careful collaborative work of medical professionals and tech-experts such as IrisVision compensate for the visual defects of the person and are programmed so as to cater for individual visual requirements.

Individuals with low vision caused by RP experience increased difficulty to see at night, termed loss of night vision. It may progress to a loss of peripheral vision, central vision and color vision as well.

Vitamins most essential for this cause include Vitamin-A, Vitamin-C, E. Milk, eggs (yolks in particular), cheese, and yogurt are a good source of vitamins

Having retinitis pigmentosa is an individual experience. It may differ for everyone. For some people, the onset of symptoms may start at an earlier age while in some cases the disease may progress at a very slow rate. Really, there is no rule of thumb for dealing with retinitis pigmentosa.

Retinitis Pigmentosa is a genetic disorder passed down from parents to their offspring. If either of the parents has a dominant gene for this disease, they have a 1 in 2 chance of passing it down to their child, whereas if both parent individuals carry the recessive gene for RP, they have a 1 in 4 chance of passing it down to their offspring.

Retinitis Pigmentosa affects the vision in three main ways:

  • Causes night blindness.
  • Causes tunnel vision
  • Vague color differentiation and acuity

No, RP rarely causes complete blindness, rather most of the people suffering from it retain some part of their central vision even after progressive deterioration of the disease over a longer time-span.

What is Retinitis Pigmentosa?

Retinitis Pigmentosa refers to a group of diseases that involve the breakdown and loss of cells in the retina.

The deterioration of the photoreceptor cells leads to a gradual loss of sight. The photoreceptor cells found in the retinal tissue are responsible for converting light into electrical impulses readable by the brain.

What Causes Retinitis Pigmentosa?

Retinitis pigmentosa is a genetic disorder, which is caused by a genetic mutation of any of the 50 different genes.

So chances of contracting the genetic disorder mainly depends upon whether your parents had it before you. Though the disorder may be rare but can result in peripheral or complete vision loss and affects about 1 in every 4,000 people in the US as reported by the National Institute of Health.

What Are The Early Symptoms of RP?

The progressive symptoms of RP vary for each patient, depending on which gene mutation has caused their condition. But symptoms of RP typically appear early on in childhood which is why some people experience rapid vision loss in early adulthood, while others may be able to retain part of their vision until late 50’s.

The effects on children can result in difficulty to see around in the dark, and it may take them a longer time to adjust to changes in lighting.

Most patients also experience photophobia; a discomfort resulting from brightly lit places.

What Does RP Look Like?

Most people with RP undergo common vision problems such as the following:

  • Night Blindness

    The loss of rod cells in the retina makes it difficult for a person to see in the dark, as well as when a person changes place from a dimly lit to a well lit environment.

  • Tunnel vision

    Tunnel vision affects the visual acuity in the peripheral vision and to put it in more simpler words, it narrows down a person’s field of vision due to the damaged rod cells in the outer layer of the retina.

Treatments of Retinitis Pigmentosa

In spite of the medical advancements, unfortunately there is no cure for Retinitis Pigmentosa. However there are treatments that can slow down the progress of disease and make it manageable. Some of the conventional treatments include:
  • Night Blindness
    The loss of rod cells in the retina makes it difficult for a person to see in the dark, as well as when a person changes place from a dimly lit to a well lit environment.

  • Tunnel vision
    As the rod cells in the outer layer of the retina get damaged, the patient also gradually loses the ability to see in their periphery.

  • Vitamin A palmitate
    In some cases, Vitamin A palmitate treatment may slow down the effects that prevent vision from further deterioration. This procedure involves taking small, periodic doses of Vitamin A palmitate if advised by an ophthalmologist or an eye specialist. More so the intake amounts of Vitamin A palmitate must also be carefully monitored as it can be harmful if taken in large amounts.

  • Retinal Implant
    A surgical procedure recommended in the later stage of RP, as it helps bring back some vision. The process requires an electrical implant to fit into the retina of the eye.
    The Argus II is an implant that is paired with glasses that restores a patient’s ability to identify objects around them. Most people with a retinal implant have a vision improvement to the extent that they can locate lights and windows in a room, and sometimes people as well.

Is there a low vision device that provides a solution for RP patients?

Yes, most certainly!!!

IrisVision smart glasses for Retinitis Pigmentosa are a breakthrough technology for RP patients, designed in collaboration with leading institutes like Johns Hopkins University, Stanford University, and UPMC Pittsburgh and leading technology corporations such as Samsung, and is the only device funded by a research grant from the National Eye Institute.

IrisVision harnesses the power of virtual reality and coupled with features of the Samsung smartphone, to restore your lost vision.

IrisVision comes with customizable features that you can adjust based on your unique visual requirements and your ease of use.

It consists of award-winning software lenses specifically designed for people with eye conditions such as RP, Glaucoma etc.

  • RP Mode
    The special ‘RP mode’ is made specifically to suit the visual needs of a person with retinitis pigmentosa. It shrinks any image to a much smaller size and fits to your field of view.

  • Colored Reading Mode
    IrisReader scans any document containing text and reads it aloud. The text is also displayed in a relatively large font with high contrast for the users to view the text as they listen.

  • Scene Mode
    IrisVision has a ‘scene mode’ which counters your tunnel vision by providing industry leading, 70 degree wide field-of-view. It has an auto-focus magnification feature which shrinks the entire picture to a smaller size and is ideal for seeing both near and far far objects.