Surgikor, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgikor, LLC - FDA 510(k) Cleared Devices
Recent clearances: Surgikor Fixation One, Abutment Blanks and Abutments, Surgikor Dental Implant System
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.
FDA 510(k) Regulatory Record - Surgikor, LLC
2 devices