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Coapt Systems, Inc.

FDA 510(k) & PMA Approved Devices — 17 products

Total Devices17
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K083783 VF LIQUIGELMIX2009-09-11 View
510(k) K080956 MODIFICATION TO VF GEL PLUSMIX2008-04-25 View
510(k) K071663 VF GEL PLUSMIX2008-02-15 View
510(k) K060248 ULTRATINE TRANSBLEPHHWC2006-06-12 View
510(k) K060249 ULTRATINE FOREHEADHWC2006-06-12 View
510(k) K060828 MODIFICATION TO ENDOTINE RIBBONGAM2006-04-19 View
510(k) K051415 ENDOTINE RIBBONGAM2005-06-23 View
510(k) K050611 ENDOTINE RIBBONGAM2005-04-06 View
510(k) K042796 ENDOTINE TRANSBLEPH 3.0/3.5 DEVICEHWC2004-11-05 View
510(k) K041835 ENDOTINE MIDFACE B 4.5 DEVICEHWC2004-09-28 View
510(k) K042078 ENDOTINE FOREHEAD TRIPLE DEVICEHWC2004-08-27 View
510(k) K040740 ENDOTINE TRANSBLEPH DEVICEHWC2004-05-10 View
510(k) K033524 COAPT ENDOTINE CHIN 3.5 DEVICEHWC2003-12-18 View
510(k) K032698 COAPT ENDOTINE MIDFACE-ST 4.5 DEVICEGAM2003-10-23 View
510(k) K032770 ENDOTINE FOREHEAD DEVICEHWC2003-10-08 View
510(k) K023922 COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197HWC2002-12-20 View
510(k) K014153 COAPT SYSTMES ENDOTINE DEVICEHWC2002-03-15 View
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