510(k) Report

FDA applicant

Microlight Corporation of America

Missouri City, TX3 decisions2002–20080 recalls

FDA records 3 decisions for Microlight Corporation of America (Missouri City, TX) from 2002 to 2008: 3 510(k) clearances. Most are in product codes ILY (Lamp, Infrared, Therapeutic Heating) and NHN (Powered Light Based Laser Non-Thermal…). Its devices cite 4 predicates, 0 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 Microlight Corporation of America’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Microlight Corporation of America 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?

  • ILYLamp, Infrared, Therapeutic Heating2decisions
  • NHNPowered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive…1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 11 times; 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.

  • K010175Microlight 830 Laser SystemMicrolight Corporation of America · 200211cite it

What has FDA decided for it lately?

  • K080786ML830TPMicrolight Corporation of America · 2008
  • K041364ML830 Laser SystemMicrolight Corporation of America · 2004
  • K010175Microlight 830 Laser SystemMicrolight Corporation of America · 2002

All 3 as Microlight Corporation of America →