Puricore, Inc.
Puricore, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2015.
Top product codes for Puricore, Inc.
Recent clearances by Puricore, Inc.
- K141863 — PURICORE WOUND HYDROGEL SPRAY DRESSING
- K131848 — VASHE WOUND SOLUTION (4.0 OZ), (8.5 OZ & (16.0 OZ)
- K123072 — VASHE WOUND THERAPY SOLUTION
- K123071 — VASHE SKIN AND WOUND HYDROGEL
- K100918 — VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014
- K093697 — VASHE WOUND THERAPY SOLUTION
- K093155 — VASHE WOUND CLEANSING SYSTEM
- K092232 — MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014
- K063159 — STERILOX LIQUID CHEMICAL STERILANT SYSTEM
- K061689 — AQUATINE EC ENDODONTIC CLEANSER
Data sourced from openFDA. This site is unofficial and independent of the FDA.