FDA applicant
Dyna Flex, Intl.
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
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.
Planning a device like Dyna Flex, Intl.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Dyna”
FDA records each applicant name separately; these may or may not be the same firm.