# Cox-Uphuff Intl.

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 11 (1980–1987): 11 510(k) clearances
- Product codes: LCJ (2), FZW (1), LFB (1), FTY (1), GCX (1), GCY (1), FZE (1), MRD (1), GEJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Allergan, Inc.: 1 (https://510kreport.com/company/allergan)
- Howmedica Corp.: 1 (https://510kreport.com/company/howmedica)

## Its most-cited devices
- K874276: Cui, Versafil (TM), Ste (TM) Tissue Expander (1987), cited by 1
- K831566: Cui Mammary Prothesis Sizer (1983), cited by 1

## Recent decisions
- K874276: Cui, Versafil (TM), Ste (TM) Tissue Expander (Dec 2, 1987)
- K874342: Ligature Carrier/Packer, Hydroxylapatite (Nov 13, 1987)
- K873470: Template (Sep 8, 1987)
- K865056: Cui Tissue Expander Versafil (TM) Tissue Expander (May 22, 1987)
- K871200: Cui Nasal Septum Button (Apr 15, 1987)
- K865033: Breast Prosthesis (Non & Inflatable) Skin Expander (Jan 12, 1987)
- K854339: Cui Chin Sizer (Nov 15, 1985)
- K853945: Cui Rhinoplasty Implants (Oct 18, 1985)

Source page: https://510kreport.com/company/cox-uphuff-intl