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Coapt Systems, Inc.

17 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
VF LIQUIGEL (K083783)Coapt Systems, Inc.2009-09-11
MODIFICATION TO VF GEL PLUS (K080956)Coapt Systems, Inc.2008-04-25
VF GEL PLUS (K071663)Coapt Systems, Inc.2008-02-15
ULTRATINE TRANSBLEPH (K060248)Coapt Systems, Inc.2006-06-12
ULTRATINE FOREHEAD (K060249)Coapt Systems, Inc.2006-06-12
MODIFICATION TO ENDOTINE RIBBON (K060828)Coapt Systems, Inc.2006-04-19
ENDOTINE RIBBON (K051415)Coapt Systems, Inc.2005-06-23
ENDOTINE RIBBON (K050611)Coapt Systems, Inc.2005-04-06
ENDOTINE TRANSBLEPH 3.0/3.5 DEVICE (K042796)Coapt Systems, Inc.2004-11-05
ENDOTINE MIDFACE B 4.5 DEVICE (K041835)Coapt Systems, Inc.2004-09-28
ENDOTINE FOREHEAD TRIPLE DEVICE (K042078)Coapt Systems, Inc.2004-08-27
ENDOTINE TRANSBLEPH DEVICE (K040740)Coapt Systems, Inc.2004-05-10
COAPT ENDOTINE CHIN 3.5 DEVICE (K033524)Coapt Systems, Inc.2003-12-18
COAPT ENDOTINE MIDFACE-ST 4.5 DEVICE (K032698)Coapt Systems, Inc.2003-10-23
ENDOTINE FOREHEAD DEVICE (K032770)Coapt Systems, Inc.2003-10-08
COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197 (K023922)Coapt Systems, Inc.2002-12-20
COAPT SYSTMES ENDOTINE DEVICE (K014153)Coapt Systems, Inc.2002-03-15

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