Sauflon Pharmaceuticals, Ltd. is one of 491 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Sauflon Pharmaceuticals, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SAUFLON CLARITI WITH TINT, SAUFLON CLARITI TORIC WITH TINT, SAUFLON CLARITI MULTIFOCAL WITH TINT, SAUFLON CLARITI (SOMOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER, SAUFLON CLARITI 1 DAY (SOMOFILCON A) SOFT (HYDROPHILIC) DAILY DISPOSABLE CONTACT LENS WITH UV BLOCKER
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.