Oculus America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculus America - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Oculus America has 1 FDA 510(k) cleared medical devices. Based in Alhambra, US.
Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculus America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oculus America
1 devices