Optixon, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Optixon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Optixon 1-Day
1
Total
1
Cleared
0
Denied
Optixon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Daegu, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Optixon, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Igc Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Optixon, Inc.
1 devices