Medical Device Manufacturer · US , Radnor , PA

Puricore, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2006

Recent clearances: PURICORE WOUND HYDROGEL SPRAY DRESSING, VASHE WOUND SOLUTION (4.0 OZ), (8.5 OZ & (16.0 OZ), VASHE WOUND THERAPY SOLUTION

View 10 510(k) Devices ↓

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Puricore, Inc. General & Plastic Surgery ✕

8 devices

1-8 of 8

Cleared May 14, 2015

PURICORE WOUND HYDROGEL SPRAY DRESSING

General & Plastic Surgery · 308d

Cleared Mar 31, 2014

VASHE WOUND SOLUTION (4.0 OZ), (8.5 OZ & (16.0 OZ)

General & Plastic Surgery · 283d

Cleared Feb 14, 2013

VASHE WOUND THERAPY SOLUTION

General & Plastic Surgery · 136d

Cleared Jan 24, 2013

VASHE SKIN AND WOUND HYDROGEL

General & Plastic Surgery · 115d

Cleared Aug 09, 2010

VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014

General & Plastic Surgery · 129d

Cleared Apr 13, 2010

VASHE WOUND THERAPY SOLUTION

General & Plastic Surgery · 134d

Cleared Mar 01, 2010

VASHE WOUND CLEANSING SYSTEM

General & Plastic Surgery · 146d

Cleared Aug 19, 2009

MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014

General & Plastic Surgery · 27d