Puricore, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Puricore, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Puricore, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Radnor, US.
Historical record: 10 cleared submissions from 2006 to 2015.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Puricore, Inc. — FDA 510(k) Products and Clearance History
10 devices
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
Cleared
Apr 02, 2007
STERILOX LIQUID CHEMICAL STERILANT SYSTEM
General Hospital
167d
Cleared
Aug 24, 2006
AQUATINE EC ENDODONTIC CLEANSER
Dental
70d