510(k) Report

FDA applicant

Diode Art Engineering Doing Business AS Air Relax

Pico Rivera, CA2 decisions2021–20210 recalls

FDA records 2 decisions for Diode Art Engineering Doing Business AS Air Relax (Pico Rivera, CA) in 2021: 2 510(k) clearances. All are in product code IRP (Massager, Powered Inflatable Tube). Its devices cite 2 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, physical medicine panel, where it files most

How often FDA has decided Diode Art Engineering Doing Business AS Air Relax’s devices, and how often a recall has named them.

FDA decisions per year

2in 2021

2021: 2
2021high 2 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Diode Art Engineering Doing Business AS Air Relax by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IRPMassager, Powered Inflatable Tube2decisions

Whose devices does it build on?

Its devices cite 2 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.

  • K211460Air Relax Plus Model AR-3.0Diode Art Engineering Doing Business AS Air Relax · 20211cites it

What has FDA decided for it lately?

  • K212491Air Relax Pro Model AR-4.0Diode Art Engineering Doing Business AS Air Relax · 2021
  • K211460Air Relax Plus Model AR-3.0Diode Art Engineering Doing Business AS Air Relax · 2021

All 2 as Diode Art Engineering Doing Business AS Air Relax →