# Precident Corp.

- Location (FDA's records): Glenview, IL
- FDA decisions: 2 (1991–1991): 2 510(k) clearances
- Product codes: EJH (1), ELR (1)
- 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
- K913019: Pdi Parallel Sided Post Kit (Oct 2, 1991)
- K911323: Flux-N-All (Sep 30, 1991)

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