Visco Vision, Inc. has 12 FDA 510(k) cleared ophthalmic devices. Based in New Taipei, Luzhou Dist, TW.

Latest FDA clearance: Oct 2026. Active since 2015.

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. 2 devices have linked clinical trials registered on ClinicalTrials.gov.

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

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