Coapt Systems, Inc.
Coapt Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2009.
Top product codes for Coapt Systems, Inc.
Recent clearances by Coapt Systems, Inc.
- K083783 — VF LIQUIGEL
- K080956 — MODIFICATION TO VF GEL PLUS
- K071663 — VF GEL PLUS
- K060248 — ULTRATINE TRANSBLEPH
- K060249 — ULTRATINE FOREHEAD
- K060828 — MODIFICATION TO ENDOTINE RIBBON
- K051415 — ENDOTINE RIBBON
- K050611 — ENDOTINE RIBBON
- K042796 — ENDOTINE TRANSBLEPH 3.0/3.5 DEVICE
- K041835 — ENDOTINE MIDFACE B 4.5 DEVICE
- K042078 — ENDOTINE FOREHEAD TRIPLE DEVICE
- K040740 — ENDOTINE TRANSBLEPH DEVICE
- K033524 — COAPT ENDOTINE CHIN 3.5 DEVICE
- K032698 — COAPT ENDOTINE MIDFACE-ST 4.5 DEVICE
- K032770 — ENDOTINE FOREHEAD DEVICE
- K023922 — COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197
- K014153 — COAPT SYSTMES ENDOTINE DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.