Oculus Innovative Sciences is one of 18402 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculus Innovative Sciences - FDA 510(k) Cleared Devices
Recent clearances: LOYON, Microcyn Plus Wound Care Solution, Microcyn Plus Skin and Wound Hydrogel
9
Total
9
Cleared
0
Denied
Oculus Innovative Sciences has 9 FDA 510(k) cleared medical devices. Based in Petaluma, US.
Historical record: 9 cleared submissions from 2013 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Oculus Innovative Sciences Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oculus Innovative Sciences
9 devices
Cleared
Mar 23, 2017
LOYON
General & Plastic Surgery
227d
Cleared
Aug 19, 2016
Microcyn Plus Wound Care Solution
General & Plastic Surgery
128d
Cleared
Apr 19, 2016
Microcyn Plus Skin and Wound Hydrogel
General & Plastic Surgery
120d
Cleared
Dec 15, 2015
Alevicyn SG Antipruritic Gel
General & Plastic Surgery
70d
Cleared
Nov 23, 2015
Ceramax Skin Barrier Cream
General & Plastic Surgery
122d
Cleared
Jun 04, 2015
Alevicyn SG Antipruritic Gel
General & Plastic Surgery
168d
Cleared
Aug 18, 2014
ENDOCYN ROOT CANAL IRRIGATION SOLUTION
Dental
87d
Cleared
Aug 08, 2014
HYDROCLEANSE WOUND CARE SOLUTION
General & Plastic Surgery
109d
Cleared
Nov 15, 2013
MICROCYN SCAR MANAGEMENT HYDROGEL
General & Plastic Surgery
162d