# Biodex Corp.

- Location (FDA's records): Shirley, NY
- FDA decisions: 7 (1986–1992): 7 510(k) clearances
- Product codes: IKK (7)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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.: 2 (https://510kreport.com/company/biodex-medical-systems)

## Its most-cited devices
- K913021: Biodex,Model B-2000 (1991), cited by 1
- K915648: Biodex System 2 Autoprogram (1992), cited by 1

## Recent decisions
- K915846: Biodex System 2 Autoprogram (Jan 13, 1992)
- K915648: Biodex System 2 Autoprogram (Jan 9, 1992)
- K913020: Biodex System 2,Model S2-S (Oct 3, 1991)
- K913021: Biodex,Model B-2000 (Oct 3, 1991)
- K900450: Biodex Lift Simulator (Jul 24, 1990)
- K900741: Biodex Back System Attachment (Feb 26, 1990)
- K860821: Biodex System (Apr 18, 1986)

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