510(k) Report

FDA applicant

Latex Medical Devices, Inc.

Brownsville, TX3 decisions1981–19900 recalls

FDA records 3 decisions for Latex Medical Devices, Inc. (Brownsville, TX) from 1981 to 1990: 3 510(k) clearances. Most are in product codes DXQ (Blood Pressure Cuff) and KNT (Tubes, Gastrointestinal (And Accessories)). 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, cardiovascular panel, where it files most

How often FDA has decided Latex Medical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Latex Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Latex Medical Devices, 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?

  • DXQBlood Pressure Cuff1decision
  • KNTTubes, Gastrointestinal (And Accessories)1decision
  • KNCTable, Obstetric (And Accessories)1decision

What has FDA decided for it lately?

  • K896986Blood Pressure CuffLatex Medical Devices, Inc. · 1990
  • K820175O.N.A.T.Latex Medical Devices, Inc. · 1982
  • K812102O.N.A.T.Latex Medical Devices, Inc. · 1981

All 3 as Latex Medical Devices, 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 Products Co., Inc. 1Latex Supply Products (Hp), Inc. 1