Visco Vision, Inc. has 11 FDA 510(k) cleared ophthalmic devices. Based in New Taipei, Luzhou Dist, TW.

Historical record: 11 cleared submissions from 2015 to 2020.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Jens Medical Consulting, Ltd. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Visco Vision, Inc.

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