FDA applicant

Metrix Teknika, Inc.

Mchenry, IL4 decisions1978–19790 recalls

FDA records 4 decisions for Metrix Teknika, Inc. (Mchenry, IL) from 1978 to 1979: 4 510(k) clearances. Most are in product codes JTC (Device, Microtiter Diluting/Dispensing) and GKT (Separator, Automated, Blood Cell, Diagnostic). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Metrix Teknika, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Metrix”

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

Metrix Co. 6

Metrix Teknika, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Metrix”