Cox-Uphuff Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cox-Uphuff Intl. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Cox-Uphuff Intl. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1980 to 1987.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cox-Uphuff Intl.
11 devices
Cleared
Dec 02, 1987
CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER
General & Plastic Surgery
43d
Cleared
Nov 13, 1987
LIGATURE CARRIER/PACKER, HYDROXYLAPATITE
General & Plastic Surgery
24d
Cleared
Sep 08, 1987
TEMPLATE
General & Plastic Surgery
11d
Cleared
May 22, 1987
CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
General & Plastic Surgery
149d
Cleared
Apr 15, 1987
CUI NASAL SEPTUM BUTTON
Ear, Nose, Throat
21d
Cleared
Jan 12, 1987
BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
General & Plastic Surgery
20d
Cleared
Nov 15, 1985
CUI CHIN SIZER
General & Plastic Surgery
18d
Cleared
Oct 18, 1985
CUI RHINOPLASTY IMPLANTS
General & Plastic Surgery
24d
Cleared
Aug 12, 1983
CUI MAMMARY PROTHESIS SIZER
General & Plastic Surgery
88d
Cleared
Jan 22, 1982
DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
General Hospital
49d
Cleared
Oct 23, 1980
COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
General & Plastic Surgery
41d