44
Total
44
Cleared
0
Denied

Ciba Vision Corporation has 44 FDA 510(k) cleared ophthalmic devices. Based in Duluth, US.

Historical record: 44 cleared submissions from 1994 to 2014.

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

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

FDA 510(k) Regulatory Record - Ciba Vision Corporation

44 devices
1-12 of 44

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