Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Coapt Systems with 17 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 2009: VF LIQUIGEL.
| Date | Record | Source |
|---|---|---|
| Sep 11, 2009 | VF LIQUIGELK083783 · MIX | 510(k) clearances |
| Apr 25, 2008 | MODIFICATION TO VF GEL PLUSK080956 · MIX | 510(k) clearances |
| Feb 15, 2008 | VF GEL PLUSK071663 · MIX | 510(k) clearances |
| Jun 12, 2006 | ULTRATINE TRANSBLEPHK060248 · HWC | 510(k) clearances |
| Jun 12, 2006 | ULTRATINE FOREHEADK060249 · HWC | 510(k) clearances |
| Apr 19, 2006 | MODIFICATION TO ENDOTINE RIBBONK060828 · GAM | 510(k) clearances |
| Jun 23, 2005 | ENDOTINE RIBBONK051415 · GAM | 510(k) clearances |
| Apr 6, 2005 | ENDOTINE RIBBONK050611 · GAM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
