510(k) Report

FDA applicant

Ezmt Valve Co., Inc.

Salinas, CA3 decisions1991–19930 recalls

FDA records 3 decisions for Ezmt Valve Co., Inc. (Salinas, CA) from 1991 to 1993: 3 510(k) clearances. Most are in product codes GAQ (Suture, Nonabsorbable, Steel, Monofilament And…) and 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 and plastic surgery panel, where it files most

How often FDA has decided Ezmt Valve Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ezmt Valve Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ezmt Valve 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?

  • GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile1decision
  • LYYLatex Patient Examination Glove1decision
  • EYZSystem, Urine Drainage, Closed, For Nonindwelling Catheter, Sterile1decision

What has FDA decided for it lately?

  • K930557Latex Examination GloveEzmt Valve Co., Inc. · 1993
  • K930556Night Urinary Drainage Bedside BagEzmt Valve Co., Inc. · 1993
  • K913155Leg UrinalEzmt Valve Co., Inc. · 1991

All 3 as Ezmt Valve Co., Inc. →