510(k) Report

FDA applicant

Techhnilab Instruments, Inc.

Mchenry, IL6 decisions1977–19810 recalls

FDA records 6 decisions for Techhnilab Instruments, Inc. (Mchenry, IL) from 1977 to 1981: 6 510(k) clearances. Most are in product codes LTB (Cyclosporine Radioimmunoassay) and ILC (Utensil, Eating). 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 chemistry panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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