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Coapt Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083783VF LIQUIGELSeptember 11, 2009
K080956MODIFICATION TO VF GEL PLUSApril 25, 2008
K071663VF GEL PLUSFebruary 15, 2008
K060249ULTRATINE FOREHEADJune 12, 2006
K060248ULTRATINE TRANSBLEPHJune 12, 2006
K060828MODIFICATION TO ENDOTINE RIBBONApril 19, 2006
K051415ENDOTINE RIBBONJune 23, 2005
K050611ENDOTINE RIBBONApril 6, 2005
K042796ENDOTINE TRANSBLEPH 3.0/3.5 DEVICENovember 5, 2004
K041835ENDOTINE MIDFACE B 4.5 DEVICESeptember 28, 2004
K042078ENDOTINE FOREHEAD TRIPLE DEVICEAugust 27, 2004
K040740ENDOTINE TRANSBLEPH DEVICEMay 10, 2004
K033524COAPT ENDOTINE CHIN 3.5 DEVICEDecember 18, 2003
K032698COAPT ENDOTINE MIDFACE-ST 4.5 DEVICEOctober 23, 2003
K032770ENDOTINE FOREHEAD DEVICEOctober 8, 2003
K023922COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197December 20, 2002
K014153COAPT SYSTMES ENDOTINE DEVICEMarch 15, 2002