Cox-Uphuff Intl.
Cox-Uphuff Intl. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1987.
Top product codes for Cox-Uphuff Intl.
Recent clearances by Cox-Uphuff Intl.
- K874276 — CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER
- K874342 — LIGATURE CARRIER/PACKER, HYDROXYLAPATITE
- K873470 — TEMPLATE
- K865056 — CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
- K871200 — CUI NASAL SEPTUM BUTTON
- K865033 — BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
- K854339 — CUI CHIN SIZER
- K853945 — CUI RHINOPLASTY IMPLANTS
- K831566 — CUI MAMMARY PROTHESIS SIZER
- K813394 — DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
- K802214 — COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.