FDA applicant

Dyna-Tek Industries

Lenexa, KS2 decisions1991–19970 recalls

FDA records 2 decisions for Dyna-Tek Industries (Lenexa, KS) from 1991 to 1997: 2 510(k) clearances. Most are in product codes DIF (Drug Mixture Control Materials) and DPA (Apparatus, General Use, Thin Layer…). 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 Dyna-Tek Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dyna-Tek Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyna-Tek Industries by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Dyna-Tek”

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

Dyna Corp. 5 Dyna Flex 4 Dyna Flex, Intl. 4 Dyna-Med 4 Dyna Industries, Inc. 2 Dyna Care 1 Dyna Dental Engineering BV 1 Dyna-Pace Systems, Inc. 1

Dyna-Tek Industries

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dyna-Tek”