Oculus Private Limited is one of 21656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculus Private Limited - FDA 510(k) Cleared Devices
Recent clearances: FRESHKON 1-DAY ALLURING EYES (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR FRESHKON 1-DAY MOSAIC (ETAFILC, FRESHKONALLURING EYES, FRESHKON COLORS FUSION, FRESHKONCOLORS FUSION SPARKLERS, FRESHKON MOSAIC, FRESHKON GLITZI
2
Total
2
Cleared
0
Denied
Oculus Private Limited has 2 FDA 510(k) cleared medical devices. Based in Greenwood Village, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculus Private Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oculus Private Limited
2 devices