Surgikor, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Surgikor, LLC has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Latest FDA clearance: Sep 2024. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Surgikor, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Surgikor, LLC
2 devices