# Dyna Flex, Intl.

- Location (FDA's records): Clinton, TN
- FDA decisions: 4 (1990–1991): 4 510(k) clearances
- Product codes: BXB (4)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K910150: Romflex Rehab Equip Extremities Unit (Jan 23, 1991)
- K910149: Romflex Rehab Equip Lateral Flexion Unit (Jan 18, 1991)
- K910151: Romflex Rehab Equip Cervical Flexor Unit (Jan 18, 1991)
- K905299: Romflex Rehabilitation Equipment (Dec 31, 1990)

Source page: https://510kreport.com/company/dyna-flex-intl