Corelink, LLC - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Corelink, LLC has 35 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Last cleared in 2023. Active since 2008.
Browse the FDA 510(k) cleared devices submitted by Corelink, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Corelink, LLC
12 devices
Cleared
Dec 08, 2023
F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and...
Orthopedic
177d
Cleared
Oct 27, 2023
CoreLink Robotic Navigation Instruments
Orthopedic
157d
Cleared
Aug 16, 2023
CoreLink Navigation Instruments
Orthopedic
30d
Cleared
Jun 06, 2023
F3D Interbody System
Orthopedic
120d
Cleared
May 02, 2023
CoreLink Navigation Instruments
Orthopedic
33d
Cleared
Mar 21, 2023
Entasis 3D Dual-Lead Sacroiliac Implant System
Orthopedic
99d
Cleared
Aug 09, 2022
NextGen Pedicle Screw System
Orthopedic
49d
Cleared
Jun 01, 2022
CoreLink Navigation Instruments
Orthopedic
58d
Cleared
Feb 04, 2022
F3D-C2 Cervical Stand-Alone System
Orthopedic
273d
Cleared
Jan 19, 2022
CoreLink Navigation Instruments
Orthopedic
23d
Cleared
Oct 13, 2021
CoreLink Navigation Instruments
Orthopedic
40d
Cleared
Apr 15, 2021
CoreLink Midline Fixation System
Orthopedic
50d