# Diality, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 2 (2024–2024): 2 510(k) clearances
- Product codes: KDI (1), FJK (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Outset Medical, Inc.: 2 (https://510kreport.com/company/outset-medical)

## Recent decisions
- K243607: Moda-flx Hemodialysis System™ Cartridge (102121-001 ) (Dec 20, 2024)
- K233798: Moda-flx Hemodialysis System and Cartridge (Aug 2, 2024)

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