FDA applicant

Dyna-Med

Victoria, TX4 decisions1976–19890 recalls

FDA records 4 decisions for Dyna-Med (Victoria, TX) from 1976 to 1989: 4 510(k) clearances. Most are in product codes JAA (System, X-Ray, Fluoroscopic, Image-Intensified) and JXL (Block, Bite). 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, radiology panel, where it files most

How often FDA has decided Dyna-Med’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dyna-Med since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyna-Med 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-Med”

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-Tek Industries 2 Dyna Industries, Inc. 2 Dyna Care 1 Dyna Dental Engineering BV 1 Dyna-Pace Systems, Inc. 1

Dyna-Med

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dyna-Med”