Essilor Intl. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Essilor Intl. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Essilor Intl. has 2 FDA 510(k) cleared medical devices. Based in Hampshire, GB.
Historical record: 2 cleared submissions from 2000 to 2004. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Essilor Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Essilor Intl.
2 devices