510(k) Report

FDA applicant

C.A.I. Industries Corp.

Alhambra, CA3 decisions1997–20040 recalls

FDA records 3 decisions for C.A.I. Industries Corp. (Alhambra, CA) from 1997 to 2004: 3 510(k) clearances. Most are in product codes MQX (Needle, Acupuncture, Single Use) and ILY (Lamp, Infrared, Therapeutic Heating). 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, general hospital panel, where it files most

How often FDA has decided C.A.I. Industries Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for C.A.I. Industries Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — C.A.I. Industries Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MQXNeedle, Acupuncture, Single Use2decisions
  • ILYLamp, Infrared, Therapeutic Heating1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 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.

  • K954577WS Frequency Spectrum Effect Physiatrics ApparatusC.A.I. Industries Corp. · 19971cites it

What has FDA decided for it lately?

  • K041652Acupuncture NeedlesC.A.I. Industries Corp. · 2004
  • K954577WS Frequency Spectrum Effect Physiatrics ApparatusC.A.I. Industries Corp. · 1997
  • K970574Acupuncture NeedlesC.A.I. Industries Corp. · 1997

All 3 as C.A.I. Industries Corp. →