What this record covers
DeveloperAppliedVR
GeographyUnited States
ModalitiesVR
StageCommercial medical device
Last reviewed2026-07-23
Clinical areas and use cases
Specialties
Pain management
Use cases
Therapy supportHome care
Regulatory context
United States: FDA Class II device record K243417. Regulatory status is region- and date-specific.
This is source-linked metadata, not an AVRMD endorsement or medical recommendation.Primary source
FDA 510(k) summary K243417Description is limited to the official indication and device summary.Questions should improve the record.
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