Regulatory
Every AR/VR device the FDA has authorized.
120 devices from 70 companies, copied from the FDA's own list and checked for changes every day. Each row links to its FDA database record.
This is the regulator's list, shown as published. FDA authorization means a device may be marketed in the US for its stated use; it is not evidence of clinical effectiveness and not an AVRMD endorsement. Source: FDA, Augmented Reality and Virtual Reality Medical Devices (FDA page updated 2026-09-04).
7 devices
- 2019-12-20xvision Spine system (XVS)Augmedics Ltd.
- 2019-11-29I-Portal Neuro Otologic Test Center, I-Portal Video Nystagmography System, I-Portal Portable Assessment System - NysragmographNeurolign USA, LLC
- 2019-08-29D2P3D Systems, Inc.
- 2019-05-13SurgicalARMEDIVIS, Inc.
- 2019-03-18REAL Immersive SystemPenumbra, Inc.
- 2019-02-22IRIS 1.0 SystemIntuitive Surgical
- 2019-02-14Presero 3D Scanning SystemCertis Health