Dk Medivision Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Dk Medivision Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TREVUES (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color)
1
Total
1
Cleared
0
Denied
Dk Medivision Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Chungcheongnam-Do, KR.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Dk Medivision Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dk Medivision Co., Ltd.
1 devices