510(k) Report

FDA applicant

Dyna Flex, Intl.

Clinton, TN4 decisions1990–19910 recalls

FDA records 4 decisions for Dyna Flex, Intl. (Clinton, TN) from 1990 to 1991: 4 510(k) clearances. All are in product code BXB (Exerciser, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Dyna Flex, Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dyna Flex, Intl. 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”

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