510(k) Report

FDA applicant

M/S Midland Latex Products, Ltd.

Eagan, MN1 decision1999–19990 recalls

FDA records 1 decision for M/S Midland Latex Products, Ltd. (Eagan, MN) in 1999: 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 M/S Midland Latex Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for M/S Midland Latex Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — M/S Midland Latex Products, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like M/S Midland Latex Products, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LYYLatex Patient Examination Glove1decision

What has FDA decided for it lately?

  • K982114Lopro Siliconised Low Protein Powderfree Latex Examination GlovesM/S Midland Latex Products, Ltd. · 1999

The one decision as M/S Midland Latex Products, Ltd. →