510(k) Report

FDA applicant

Maytex Corp.

Hayward, CA4 decisions1989–19940 recalls

FDA records 4 decisions for Maytex Corp. (Hayward, CA) from 1989 to 1994: 4 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 Maytex Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maytex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Maytex 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?

  • LYYLatex Patient Examination Glove4decisions

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.

  • K935315Maytex Powder-Free Latex Examination GlovesMaytex Corp. · 19941cites it

What has FDA decided for it lately?

  • K935314Maytex Latex Examination Gloves, PowderedMaytex Corp. · 1994
  • K935315Maytex Powder-Free Latex Examination GlovesMaytex Corp. · 1994
  • K892082Maytex Non-Sterile Latex Exam GlovesMaytex Corp. · 1989
  • K892183Maytex Latex Examination GlovesMaytex Corp. · 1989

All 4 as Maytex Corp. →