Ocusense, Inc. is one of 24854 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ocusense, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TEARLAB OSMOLARITY SYSTEM
1
Total
1
Cleared
0
Denied
Ocusense, Inc. has 1 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ocusense, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Ocusense, Inc.
1 devices