# Sez Corporation

- Location (FDA's records): Deerfield, IL
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: MEG (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Exelint Intl. Co.: 1 (https://510kreport.com/company/exelint-intl)

## Firms that cite its devices most
- Medexel Medical Mfg. Co., Ltd.: 1 (https://510kreport.com/company/medexel-medical-mfg)
- Uniqsafe Biomeditech Co., Ltd.: 1 (https://510kreport.com/company/uniqsafe-biomeditech)
- Vitalcare Group, Inc.: 1 (https://510kreport.com/company/vitalcare-group)
- Dolomite Biotech Sdn Bhd: 1 (https://510kreport.com/company/dolomite-biotech-sdn-bhd)

## Its most-cited devices
- K031163: Sez Safety Syringe (2003), cited by 4

## Recent decisions
- K031163: Sez Safety Syringe (Jul 8, 2003)

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