510(k) Report

FDA applicant

Latex Products Co., Inc.

Metro Manilla, PH1 decision1989–19890 recalls

FDA records 1 decision for Latex Products Co., Inc. (Metro Manilla, PH) in 1989: 1 510(k) clearance. 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 Latex Products Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Latex Products Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Latex Products Co., 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?

  • LYYLatex Patient Examination Glove1decision

What has FDA decided for it lately?

  • K891265Latexco Latex Examination GlovesLatex Products Co., Inc. · 1989

The one decision as Latex Products Co., Inc. →

Other applicant names beginning “Latex”

FDA records each applicant name separately; these may or may not be the same firm.

Latex Ind., Inc. 14Latex Medical Devices, Inc. 3Latex Supply Products (Hp), Inc. 1