Oculight , Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Oculight , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Nam illumination probe with chopper
1
Total
1
Cleared
0
Denied
Oculight , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Last cleared in 2021. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculight , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Oculight , Ltd.
1 devices