Coapt Systems, Inc.
FDA 510(k) medical device clearances.
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.