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).
5 devices
- 2022-12-30Cyware 4H and Cysart 4HAbys Medical
- 2022-11-25VSI HoloMedicineApoQlar GmbH
- 2022-10-21IntraOp VSP Software DeviceXironetic, LLC
- 2022-07-29OptiVu ROSA MxROrthosoft, Inc. (d/b/a Zimmer CAS)
- 2022-06-15SurgiCase ViewerMaterialise NV