Facility

APPLIEDVR

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3021071568
Establishment type	Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Location	16760 Stagg St Unit 216 Van Nuys, CA, US 91406
Registration status	Active · expires 2026
Parent company	AppliedVR (owner-operator 10083591)
Brand names	RelieVRx

Activity by year

Recalls (1)

Devices registered here (1)

Virtual Reality Behavioral Therapy Device For Pain Relief
Product code QRA (opens in a new tab) · Class II · Neurology · 21 CFR 890.5800

Recalls & enforcement

Class IICompleted2023-02-27
There is the potential for the program software to malfunction which will not allow it to move forward to the next session.

All facilities operated by AppliedVR

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “APPLIEDVR (FEI 3021071568) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3021071568-appliedvr/

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