Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Cox-Uphuff International with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 2, 1987: CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER.
| Dec 2, 1987 | CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDERK874276 · FZW | 510(k) clearances |
| Nov 13, 1987 | LIGATURE CARRIER/PACKER, HYDROXYLAPATITEK874342 · GEJ | 510(k) clearances |
| Sep 8, 1987 | TEMPLATEK873470 · FTY | 510(k) clearances |
| May 22, 1987 | CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDERK865056 · LCJ | 510(k) clearances |
| Apr 15, 1987 | CUI NASAL SEPTUM BUTTONK871200 · LFB | 510(k) clearances |
| Jan 12, 1987 | BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDERK865033 · LCJ | 510(k) clearances |
| Nov 15, 1985 | CUI CHIN SIZERK854339 · | 510(k) clearances |
| Oct 18, 1985 | CUI RHINOPLASTY IMPLANTSK853945 · FZE | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
