Clevaligner, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Clevaligner, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Jerusalem, IL.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Clevaligner, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rs Ness as regulatory consultant.
FDA 510(k) Regulatory Record - Clevaligner, Ltd.
1 devices