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ODs on Finance

Think you know ERG? Think again

RETeval Device: ERG Simplified

Electroretinography isn’t what it used to be. FDA-cleared and made in the US, the RETeval® offers a portable, handheld solution that is comfortable for patients, easy for clinicians, and provides an efficient, objective functional assessment of retinal health.

With our exclusive offer for ODs on Finance members, the RETeval handheld ERG can benefit both patients and practice.

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Why RETeval?

Designed with you in Mind

  • Testing on both eyes can be completed in only a few minutes
  • Portable, handheld device can be used anywhere in your clinic
  • Color-coded report simplifies interpretation
  • Age-matched reference database helps stratify patient results

Comfortable for Patients

  • Patented Sensor Strip™ adhesive skin electrodes save time & reduce hassle
  • Flexible Sensor Strip material is gentle on skin with no corneal contact required
  • Appropriate for any age without sedation
  • Dilation not required

Novel practice builder

  • Reimbursable with CPT code 92273
  • More than 560 applicable ICD-10 codes
  • Seamlessly integrates into clinic workflow with minimal training
  • Accessible investment to fuel practice growths

ERG Coding & Reimbursement Guide >

Catch the Latest Wave of Functional Assessment

Diabetic Retinopathy

Diabetic Retinopathy

The RETeval’s DR Assessment Protocol predicts your patient’s risk for progression to inform your treatment protocols and guide referral timing.

Detect Progression Risk
Glaucoma

Glaucoma

Aid and support the diagnosis, management, and treatment of glaucoma by detecting and tracking chnges to the ganglion cell layer with the RETeval’s PhNR protocol.

Measure Ganglion Cell Function
"We've found that the RETeval has been an efficient and portable tool for early diagnosis in retinopathy and glaucoma. Our profits have increased by over $50,000 per year since adding the RETeval to the office. It has been a truly remarkable addition to our medical optometric practice!"
Henry D. Patterson
Henry D. PattersonOptometrist
Electroretinography (ERG) Coding and Reimbursement Guide

ERG & VEP Coding and Reimbursement Guides

In the United States, there are more than 600 ICD-10 codes that may be associated with the CPT codes used to report electroretinography and visual-evoked potential. That list can be found at CMS.gov. The following guides provided by The Pinnacle Health Group lists some of the more common ICD-10 diagnosis codes that may be used for protocols associated with the RETeval handheld device.

Download ERG Giude
Download VEP Giude

The above guides focus on Physician Office Coding and Reimbursement. For Hospital Outpatient guides, please contact us here.

"I have been using the RETeval for almost a year now. It's super easy for staff to use, patients think it's cool, and it helps me with clinical decision making. It has really good reimbursement. Highly recommend."
Jeff Binstock
Jeff BinstockOptometrist

Backed by Science

Validated by 200+ Peer-Reviewed Research Studies

Since its launch in 2015, more than 3,000 devices have been installed worldwide in optometry, ophthalmology, retina specialty, and research settings. LKC Technologies has been an industry leader in functional assessments for more than 45 years, and the RETeval is backed by science – giving you peace of mind that you’re making the right choice for your patients.

Dive into the research

How It Works

The RETeval device will start flashing light into the patient's eye.

The retina responds to the flashes by generating small electrical signals that travel through the facial structure to the Sensor Strip.

The Sensor Strip detects the electrical signals and compares the results to the age-adjusted reference database.

Watch Instructional Video

Let’s Talk!

Request a demo or more information about the RETeval device.
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© 2024 LKC Technologies, Inc.

California Proposition 65 information

Prop-65Warning: This product can expose you to chemicals including lead, which is known to the State of California to cause cancer and birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.

Substance Tables:

The table below lists substances which may be contained within LKC’s RETeval and RETevet products. Substances listed as Type 1 are within permissible levels in one or more of LKC’s products. Substances listed as Type 2 are used in the production of some components used in LKC products and may be present at trace levels, but are typically destroyed during processing. 

RETeval and RETevet Devices

Substance CAS # Type Listed as causing:
Nickel 7440-02-0 1 Cancer
Acrylonitrile 107-13-1 2
Ethylbenzine 100-41-4 2
Crystaline Silica 14808-60-7 1
Lead 7439-92-1 1 Cancer Developmental Toxicity Male Reproductive Toxicity Female Reproductive Toxicity
Methylene Chloride 75-09-2 2 Cancer Female Reproductive Toxicity
Bisphenol A 80-05-7 2
N-Hexane  110-54-3 2 Male Reproductive Toxicity