510(k) Report

FDA applicant

Appliedvr

Van Nuys, CA3 decisions2021–20250 recalls

FDA records 3 decisions for Appliedvr (Van Nuys, CA) from 2021 to 2025: 2 510(k) clearances and 1 De Novo grant. All are in product code QRA (Virtual Reality Behavioral Therapy Device For…). Its devices cite 2 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Appliedvr, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Appliedvr’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2021: 12024: 12025: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Appliedvr by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Appliedvr’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • QRAVirtual Reality Behavioral Therapy Device For Pain Relief3decisions

Who builds on its devices?

Later devices cite its devices 4 times; 2 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • DEN210014EaseVRxAppliedvr, Inc. · 20213cite it
  • K243417RelieVRxAppliedvr · 20241cites it

What has FDA decided for it lately?

All 2 as Appliedvr →The one decision as Appliedvr, Inc. →