Prugen IP Holdings, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prugen IP Holdings, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Prugen IP Holdings, Inc. has 6 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Historical record: 6 cleared submissions from 2010 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Prugen IP Holdings, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prugen IP Holdings, Inc.
6 devices
Cleared
Feb 09, 2012
HPR EMOLLIENT FOAM
General & Plastic Surgery
49d
Cleared
Feb 09, 2012
HPR PLUS EMOLLIENT FOAM
General & Plastic Surgery
49d
Cleared
Jun 03, 2011
EMULSION SB
General & Plastic Surgery
79d
Cleared
Jun 24, 2010
PRUCLAIR NONSTEROIDAL CREAM
General & Plastic Surgery
261d
Cleared
Jun 24, 2010
PR CREAM
General & Plastic Surgery
261d
Cleared
Jan 15, 2010
PRUTECT TOPICAL OINTMENT, MODELS 45 GRAM TUBE, 90 GRAM TUBE
General & Plastic Surgery
119d