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 PuriCore with 10 510(k) clearances. The most recent is a 510(k) clearance dated May 14, 2015: PURICORE WOUND HYDROGEL SPRAY DRESSING.
| May 14, 2015 | PURICORE WOUND HYDROGEL SPRAY DRESSINGK141863 · FRO | 510(k) clearances |
| Mar 31, 2014 | VASHE WOUND SOLUTION (4.0 OZ), (8.5 OZ & (16.0 OZ)K131848 · FRO | 510(k) clearances |
| Feb 14, 2013 | VASHE WOUND THERAPY SOLUTIONK123072 · FRO | 510(k) clearances |
| Jan 24, 2013 | VASHE SKIN AND WOUND HYDROGELK123071 · FRO | 510(k) clearances |
| Aug 9, 2010 | VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014K100918 · FRO | 510(k) clearances |
| Apr 13, 2010 | VASHE WOUND THERAPY SOLUTIONK093697 · FRO | 510(k) clearances |
| Mar 1, 2010 | VASHE WOUND CLEANSING SYSTEMK093155 · FRO | 510(k) clearances |
| Aug 19, 2009 | MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014K092232 · FRO | 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
