# Cui Corp.

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 7 (1990–1991): 7 510(k) clearances
- Product codes: LZK (2), FZE (2), FWP (2), MDA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Target Health, Inc.: 1 (https://510kreport.com/company/target-health)

## Its most-cited devices
- K913140: Silicone Gel Sheeting (1991), cited by 1

## Recent decisions
- K913140: Silicone Gel Sheeting (Sep 30, 1991)
- K904350: Cui Dorsal Columella Prosthesis (Nov 26, 1990)
- K904348: Cui Feathered Silicone Malar (Nov 26, 1990)
- K904349: Cui Curvilinear Silicone Chin (Nov 26, 1990)
- K903329: Cui Anatomical Silicone Malar (Sep 10, 1990)
- K903328: Cui Premaxillary Implant (Sep 10, 1990)
- K903327: Cui Articulated Silicone Chin (Sep 10, 1990)

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