# Simergent, LLC

- Location (FDA's records): Oklahoma City, OK
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: FKX (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
- Fresenius Medical Care North America: 1 (https://510kreport.com/company/fresenius-medical-care-north-america)
- American Medical Products, Inc.: 1 (https://510kreport.com/company/american-medical-products)

## Recent decisions
- K250523: Archimedes Pro Automated Peritoneal Dialysis Cycler (3014-00000-1); Archimedes Standard Automated Peritoneal Dialysis Cycler (3014-00000-3); Archimedes Pro Disposable Tubing Set (3014-50000-1); Archimedes Standard Disposable Tubing Set (3014-50000-3); Archimedes Pro Plus Disposable Tubing Set (3014-50000-5) (Oct 2, 2025)

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