RelieVRx

Appliedvr, Inc. · Model RVX-2001 · UDI-DI 00850038247010

QRA Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).

Recalls

Date	Firm	Reason
2023-02-27	Appliedvr	There is the potential for the program software to malfunction which will not allow it to move forward to the next session.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.