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 14, 2026, FDA's public records list Cormatrix Cardiovascular with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 10, 2018: CorMatrix Cor Patch (3 cm x 5 cm)(single pack), CorMatrix Cor Patch (4 cm x 7 cm)(single….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 10, 2018 | CorMatrix Cor Patch (3 cm x 5 cm)(single pack), CorMatrix Cor Patch (4 cm x 7 cm)(single pack), CorMatrix Cor Patch (7 cm x 10 cm)(single pack)K181038 · PSQ | 510(k) clearances |
| Feb 4, 2016 | CorMatrix TykeK152127 · DXZ | 510(k) clearances |
| Aug 15, 2014 | CORMATRIX PROTECT ECM ENVELOPEK140306 · FTM | 510(k) clearances |
| Jul 15, 2014 | CORMATRIX ECM FOR VASCULAR REPAIRK140789 · DXZ | 510(k) clearances |
| Jul 26, 2011 | PATCH, PLEDGET AND INTRACARDIACK111187 · DXZ | 510(k) clearances |
| Feb 16, 2007 | CORMATRIX PATCH FOR CARDIAC TISSUE REPAIRK063349 · DXZ | 510(k) clearances |
| Aug 31, 2005 | REGENSIS PERICARDIAL PATCHK051405 · DXZ | 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
