510(k) Report

FDA applicant

Vision Quest Industries Inc./Dba VQ Orthocare

Vista, CA2 decisions2019–20200 recalls

FDA records 2 decisions for Vision Quest Industries Inc./Dba VQ Orthocare (Vista, CA) from 2019 to 2020: 2 510(k) clearances. Most are in product codes LIH (Interferential Current Therapy) and IPF (Stimulator, Muscle, Powered). Its devices cite 4 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

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 Vision Quest Industries Inc./Dba VQ Orthocare’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2019: 12020: 1
2019high 1 (2019) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Vision Quest Industries Inc./Dba VQ Orthocare by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LIHInterferential Current Therapy1decision
  • IPFStimulator, Muscle, Powered1decision

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K183692Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare · 20191cites it

What has FDA decided for it lately?

  • K202490Avid CT2Vision Quest Industries Inc./Dba VQ Orthocare · 2020
  • K183692Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare · 2019

All 2 as Vision Quest Industries Inc./Dba VQ Orthocare →