Coapt Systems, Inc.

Medical device manufacturer in Palo Alto, CA.

17510(k) clearances
0PMA approvals
0recalls

Device types

510(k) clearances

510(k)DeviceDecision
K083783VF LiquigelMIX · Traditional 09/11/2009SE
K080956Modification to VF Gel PlusMIX · Special 04/25/2008SE
K071663VF Gel PlusMIX · Traditional 02/15/2008SE
K060249Ultratine ForeheadHWC · Traditional 06/12/2006SE
K060248Ultratine TransblephHWC · Traditional 06/12/2006SE
K060828Modification to Endotine RibbonGAM · Special 04/19/2006SE
K051415Endotine RibbonGAM · Traditional 06/23/2005SE
K050611Endotine RibbonGAM · Special 04/06/2005SE
K042796Endotine Transbleph 3.0/3.5 DeviceHWC · Special 11/05/2004SE
K041835Endotine Midface B 4.5 DeviceHWC · Traditional 09/28/2004SE
K042078Endotine Forehead Triple DeviceHWC · Special 08/27/2004SE
K040740Endotine Transbleph DeviceHWC · Traditional 05/10/2004SE
K033524Coapt Endotine Chin 3.5 DeviceHWC · Traditional 12/18/2003SE
K032698Coapt Endotine Midface-St 4.5 DeviceGAM · Traditional 10/23/2003SE
K032770Endotine Forehead DeviceHWC · Special 10/08/2003SE
K023922Coapt Systems Endotine Device, Model CFD-101-00197HWC · Special 12/20/2002SE
K014153Coapt Systmes Endotine DeviceHWC · Traditional 03/15/2002SE