Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Syncthink, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2021-10-02
TypeNumberDevice NameCodeDateActions
510(k) K202927 EYE-SYNCQEA2021-10-02 View
510(k) K152915 EYE-SYNCGWN2016-01-29 View