# Cypris Medical

- Location (FDA's records): Chicago, IL
- FDA decisions: 2 (2024–2024): 2 510(k) clearances
- Product codes: GEJ (1), GAW (1)
- Predicates its devices cite: 3 (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
- Surgical Specialties Corp: 2 (https://510kreport.com/company/surgical-specialties)
- Surgical Specialties Corp. Dba Angiotech: 1 (https://510kreport.com/company/surgical-specialties-dba-angiotech)

## Recent decisions
- K240185: Cypris eXact Suture Placement Device (May 3, 2024)
- K233355: Cypris eXact Suturing System (Jan 12, 2024)

Source page: https://510kreport.com/company/cypris-medical