510(k) Report

FDA applicant

Jda Intl., Inc.

Ontario, CA1 decision1999–19990 recalls

FDA records 1 decision for Jda Intl., Inc. (Ontario, CA) in 1999: 1 510(k) clearance. All are in product code LZA (Polymer 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 Jda Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jda Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jda Intl., Inc. 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?

  • LZAPolymer Patient Examination Glove1decision

Who builds on its devices?

Later devices cite its devices 7 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.

  • K993247Nitrile Powder Free Patient Examination GlovesJda Intl., Inc. · 19997cite it

What has FDA decided for it lately?

  • K993247Nitrile Powder Free Patient Examination GlovesJda Intl., Inc. · 1999

The one decision as Jda Intl., Inc. →