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.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
2 devices