FDA applicant

Cox-Uphuff Intl.

Santa Barbara, CA11 decisions1980–19873 recalls

FDA records 11 decisions for Cox-Uphuff Intl. (Santa Barbara, CA) from 1980 to 1987: 11 510(k) clearances. Most are in product codes LCJ (Tissue Expander And Accessories) and FZW (Expander, Surgical, Skin Graft). 3 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Cox-Uphuff Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cox-Uphuff Intl. since 2007.

Recalls per year

1in 2019

2007high 2 (2015) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Cox-Uphuff Intl. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cox-Uphuff Intl.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Cox-Uphuff Intl.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?