# Cybex

- Location (FDA's records): Ronkonkoma, NY
- FDA decisions: 9 (1984–1995): 9 510(k) clearances
- Product codes: IKK (7), ISD (1), KQX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Biodex Medical Systems, Inc.: 1 (https://510kreport.com/company/biodex-medical-systems)

## Its most-cited devices
- K905525: CYBEX 6000 (1991), cited by 1

## Recent decisions
- K950095: CYBEX 770 (Jun 21, 1995)
- K905525: CYBEX 6000 (Feb 14, 1991)
- K881681: Cybex Back Testing and Rehabilitation System (Apr 25, 1990)
- K881676: Linear Lift Device (Apr 25, 1990)
- K894154: Metabolic Systems (Oct 24, 1989)
- K873599: EDI 320 (Oct 16, 1987)
- K872911: CYBEX 340 (Sep 24, 1987)
- K844368: Linear Lift Device (Feb 19, 1985)

Source page: https://510kreport.com/company/cybex