510(k) Report

FDA applicant

Texas Instruments, Inc.

Mchenry, IL3 decisions1976–19860 recalls

FDA records 3 decisions for Texas Instruments, Inc. (Mchenry, IL) from 1976 to 1986: 3 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and FLL (Continuous Measurement Thermometer). 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, neurology panel, where it files most

How often FDA has decided Texas Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Texas Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Texas Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Texas Instruments, Inc.’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?

  • GXYElectrode, Cutaneous1decision
  • FLLContinuous Measurement Thermometer1decision
  • ILQSystem, Communication, Powered1decision

What has FDA decided for it lately?

  • K864204Vocaid, Electronic Vocal AidTexas Instruments, Inc. · 1986
  • K761255Digital ThermometerTexas Instruments, Inc. · 1977
  • K760947Pregelled Disposable ElectrodeTexas Instruments, Inc. · 1976

All 3 as Texas Instruments, Inc. →