Vision Science Co., Ltd. is one of 13027 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vision Science Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, ISENS (POLYMACON) SPHERICAL AND TORIC DAILY WEAR SOFT CONTACT LENSES (CLEAR, TINTED, AND COSMETIC TINTED)
2
Total
2
Cleared
0
Denied
Vision Science Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Beaverton, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vision Science 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 - Vision Science Co., Ltd.
2 devices