Twilight™ Dark Adaptometer

Turn vague patients' complaints of night vision loss into a precise biomarker.

The Twilight™ Dark Adaptometer is an FDA-registered Class I portable diagnostic device that objectively measures how quickly the retina recovers from a standardized bleaching light. The test detects retinal dysfunction long before standard imaging scans show anatomical damage.

The portable, cloud-connected system fits into the clinical workflow without a dedicated dark room. It offers:

  • Objective dark-adaptation measurement and interpretable curves
  • Rapid and extended testing protocols
  • Lightweight headset and simple patient-friendly console
  • Results available through HIPAA-compliant SightGard™ Cloud

Standard imaging tests provide detailed structural information. Twilight measures a functional process—how retinal sensitivity recovers after photobleaching. The two approaches are complementary, and Twilight can discover retinal dysfunction up to 3 years before the structural damage is visible in imaging.

Twilight Dark Adaptometer headset and console
Designed for Eye Clinics

Practical Deployment For Busy Eye Clinics

The Twilight™ Dark Adaptometer eliminates barriers to adoption, such as dark rooms, need for dilation, lengthy exams or heavy headsets, making dark adaptation testing practical for any primary eye care practice.

The device utilizes the 3LRI Protocol™, a proprietary method that measures rod-mediated dark adaptation in 6.5 minutes or less of active testing.

The clinical workflow is designed to be simple and technician-light:

  • No Dark Room Required: The specialized eye mask handles ambient light, eliminating the need for a dedicated dark room.
  • No Dilation: Patients undergo the exam comfortably without undergoing dilation.
  • Audio-Guided Testing: The device guides the patient through the test with clear voice prompts, reducing staff supervision time.
  • Intuitive Response: Patients respond using a simple two-button handset featuring a haptic click.
  • Photostimulus Verification: An integrated photodiode to verify completeness of the dark environment and record any light leakage during tests.
  • Support for Medical Billing:The built-in Medical Necessity Survey helps staff identify qualifying symptoms and medical history during intake, automatically documenting the clinical necessity of the diagnostic or screening exam.

Cloud-Connected and AI-Ready

Every dark adaptation recovery curve is captured continuously and uploaded automatically to SightGard™, EVOQ's HIPAA-compliant cloud analytics platform.

Rather than capturing only point-of-time data, SightGard™ structures the recovery curve and derives key metrics, including the 3LRI crossing (the time it takes the retina to recover 3.0 log units). The platform stores these measurements to build a secure longitudinal record for each patient. As the patient returns for follow-up testing, clinicians can easily compare new results against their historical baseline to monitor changes in retinal function over time.

Built with the future of functional diagnostic medicine in mind, the cloud-native SightGard™ data layer is fully AI-ready, structured to support future advanced analytics and predictive modeling.

SightGard Twilight dark adaptation curve output showing 3LRI metric

In the Rapid protocol, recovery that does not reach the 3LRI within 6.5 minutes is identified as abnormal. Results should be interpreted together with the patient's symptoms, history, risk factors, clinical examination, and other diagnostic findings.

Follow the five-step workflow built for seamless delegation to practice technicians.

Prepare

Enter or confirm patient information, select the eye and protocol, and position the light-blocking eye mask.

Medical Necessity Survey

Patient to respond to questions that help to establish if their test may qualify for reimbursement.

Photobleach

Twilight delivers a controlled stimulus while an integrated photodiode monitors exposure to verify integrity.

Measure Recovery

The patient uses a two-button handset to indicate whether each stimulus is seen. Audio prompts and haptic feedback guide the patient.

Review and Follow

The test curve, recovery metrics, and test results are securely transferred to SightGard™ Cloud for review.

Select Between Two Protocols

Standard Test

Rapid Protocol

Designed for efficient clinical assessment of recovery to the 3LRI criterion, with a maximum duration of 6.5 minutes after photobleaching. This protocol gives an answer to the question if dark adaptation is normal or abnormal (delayed).

Longer Test

Extended Monitoring

Continues the recovery curve for up to 15 minutes when the rapid test is abnormal and a doctor needs to know how much the dark adaptation is delayed.

Specifications

Technical Overview

Modality
Dark-adaptation and retinal sensitivity-recovery assessment
Test Format
Monocular, psychophysical test
Workflow
Portable clinical system; no dedicated dark room required
Patient Response
Two-button Yes/No handheld controller with haptic feedback
Control Interface
Android clinical console with audio-guided prompts
Results Output
Test results, adaptation curve, 3LRI, curve analysis, photodiode light leakage monitoring
Protocols
Rapid (max 6.5 min) and extended monitoring (max 15 min) options
Connectivity
SightGard™ Cloud integration
Longitudinal Results Review
Available for authorized users through SightGard™
Patient Interface
Single-use light-blocking eye mask
Patient Selection

Five Patient Types Can Benefit From Dark Adaptation Test

  • Adults 50 years of age and older
  • Patients with family history or early signs of AMD
  • Patients with diabetes, even without visible retinopathy
  • Patients reporting night vision or low light difficulties
  • Patients on chronic medications with known retinal toxicity

Twilight does not replace the comprehensive eye examination or structural imaging. It adds a different dimension: an objective measurement of retinal recovery under low-light conditions.

The Economics

New Revenue Stream For Eye Clinics

The diagnostic dark adaptation examination with interpretation and report is reimbursable under CPT® 92284. Coverage policies vary by payor, so each practice must check the reimbursement levels and limitations with their respective Medicare Administrative Contractors (MACs) and private insurers.

The screening dark adaptation examination with interpretation and report falls under the CPT® 92288, and is not reimbursed by Medicare. However, some private payors reimburse it. Practices are responsible for verifying the requirements.

To support practice billing compliance, the on-device Medical Necessity Survey walks the patient through standard medical history questions. This survey automatically establishes the clinical necessity of the test for the medical record, lowering the risk of claim rejection.

Most primary eye care practices do not currently offer dark adaptation testing, meaning the vast majority of symptomatic patients over age fifty go untested. Adopting the Twilight™ Dark Adaptometer allows a clinic to fill an important gap in patient care while establishing an immediate revenue stream.

The financial model is structured for rapid practice payback:

  • Accessible Price: The Twilight™ standard system price is $9,799, plus the price of cloud subscription and eye masks.
  • Reimbursement: Diagnostic dark adaptation testing under CPT® 92284 reimburses between $27 to $105 per exam for a qualifying patient, varying based on region and payer policies.
  • Under One Year ROI at Two Tests on Average Per Day:Practices can fully recover their capital equipment and operating costs in less than twelve months, at two tests on average per day.

An interactive ROI Calculator is available to run practice-specific inputs and model your exact ROI based on your patient population.

Protect Your Patients' Vision and Your Practice's Future

Learn what a dark adaptation test can reveal for your patients and explore how Twilight™ fits into your clinical workflow.

Request a Live Walkthrough:Schedule a video call with our team for a live demonstration of the Twilight™ device and the SightGard™ cloud platform. You will see the SightGard™ dashboard in action and we will walk you through the structure of dark adaptation curves and how longitudinal comparative reports are generated.

Request a Sample Patient Report:Request a copy of an anonymized patient report. See exactly how the 3LRI slope metrics are presented for easy clinical review.

Model Your Practice's ROI: Run the ROI Calculator using your clinic's specific patient population to see how you can achieve a payback in under one year.

Twilight™ is intended for use by qualified eye care professionals in accordance with its current labeling and instructions for use. Test results should be interpreted in the context of the complete clinical evaluation.

CPT is a registered trademark of the American Medical Association.