Synergeyes, Inc. has 9 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 9 cleared submissions from 2006 to 2016. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Synergeyes, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by R.E. Lippman Regulatory Pathways and Eyereg Consulting, Inc..

FDA 510(k) Regulatory Record - Synergeyes, Inc.

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