OculoMotor Technologies

VERVE is software that provides virtual-reality vision exercises for convergence insufficiency. The system presents visual targets through a tablet and VR headset, while integrated eye…

Registry build 21.09.26

VERVE is software that provides virtual-reality vision exercises for convergence insufficiency. The system presents visual targets through a tablet and VR headset, while integrated eye tracking measures eye movement during the exercise. The headset-based interaction places exercises in a virtual visual scene.

The filed model is the VERVE system from OculoMotor Technologies. It combines software, a display headset and eye-tracking input as a guided vision-exercise platform.

Listed Item

Virtual Eye Rotation Vision Exercises for Convergence Insufficiency Therapy

Virtual Exercise System

The virtual environment presents targets that the user views while the system tracks eye movement. These inputs support the software’s vision-exercise interaction.

The device is described as vision-therapy software for convergence insufficiency.

1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Hunan.

Chinese manufacturers registered for FDA product code SBN
Manufacturer City Province Registered as Device types
Changsha Airdoc Health Technology Co., Ltd. Changsha Hunan Contract manufacturer 2

Record

Regulatory record for OculoMotor Technologies
Listed by Oculomotor Technologies, United States
FDA product code SBN
Device type Digital Therapy Device For Convergence Insufficiency
Device class Class 1
Regulation 21 CFR 886.1290
510(k) K232930
Record published 2025-01-28
Record revised 2026-03-19 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, serial number

Catalogue Numbers

Catalogue numbers for OculoMotor Technologies
Catalogue number Size Status
VERVE In distribution

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232930 2024-06-13

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

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5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer