Neo Vision Co., Ltd. is one of 464 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Neo Vision Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Neo Cosmo (Polymacon) Soft (Hydrophilic) Contact Lens
1
Total
1
Cleared
0
Denied
Neo Vision Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Neo Vision Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Albert Rego PHD as regulatory consultant.
FDA 510(k) Regulatory Record - Neo Vision Co., Ltd.
1 devices