Scilex, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Scilex, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Scilex, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Rishon Le Zion, IL.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Scilex, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scilex, Ltd.
1 devices