510(k) Report

FDA applicant

Technical Resources, Inc.

Mchenry, IL3 decisions1979–19810 recalls

FDA records 3 decisions for Technical Resources, Inc. (Mchenry, IL) from 1979 to 1981: 3 510(k) clearances. Most are in product codes DIT (Thin Layer Chromatography, Amphetamine) and GES (Blade, Scalpel). 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, clinical toxicology panel, where it files most

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

FDA decisions per year

No FDA decision for Technical Resources, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Technical Resources, 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?

  • DITThin Layer Chromatography, Amphetamine1decision
  • GESBlade, Scalpel1decision
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

What has FDA decided for it lately?

  • K810572Blade, Handle, Scalpel Forceps, SurgeryTechnical Resources, Inc. · 1981
  • K792473Therapette, Model NO MH-100Technical Resources, Inc. · 1979
  • K790805Drug Abuse DipsticksTechnical Resources, Inc. · 1979

All 3 as Technical Resources, Inc. →

Other applicant names beginning “Technical”

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

Technical Products, Inc. 6Technical Medical Products, Inc. 3Technical Associates of New England 1Technical Devices For Medicine 1Technical Enginuities Co. 1