Oculus Innovative Sciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculus Innovative Sciences, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Oculus Innovative Sciences, Inc. has 7 FDA 510(k) cleared medical devices. Based in Petaluma, US.
Historical record: 7 cleared submissions from 2005 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Oculus Innovative Sciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oculus Innovative Sciences, Inc.
7 devices
Cleared
Feb 02, 2011
PEDIACYN ATOPIC DERMATITIS HYDROGEL
General & Plastic Surgery
121d
Cleared
Mar 08, 2010
MICROCYN SKIN AND WOUND HYDROGEL
General & Plastic Surgery
109d
Cleared
Jun 02, 2009
OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER
General & Plastic Surgery
125d
Cleared
May 20, 2009
OCULUS MICROCYN WOUND GEL
General & Plastic Surgery
62d
Cleared
Feb 22, 2006
DERMACYN WOUND CARE
General & Plastic Surgery
36d
Cleared
May 17, 2005
DERMACYN WOUND IRRIGATION
General & Plastic Surgery
228d
Cleared
May 03, 2005
MICROCYN WOUND CARE DRESSING
General & Plastic Surgery
365d