12
Total
12
Cleared
0
Denied

Sauflon Pharmaceuticals, Ltd. has 12 FDA 510(k) cleared ophthalmic devices. Based in Twickenham, Middlesex, GB.

Historical record: 12 cleared submissions from 1999 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.

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

FDA 510(k) Regulatory Record - Sauflon Pharmaceuticals, Ltd.

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