Curiteva, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curiteva, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Curiteva Porous PEEK Cervical Interbody System, Curiteva Porous PEEK Cervical Interbody Fusion System, Curiteva Porous PEEK Standalone ALIF System
11
Total
11
Cleared
0
Denied
Curiteva, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Tanner, US.
Latest FDA clearance: Jan 2026. Active since 2019.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp and Mcra, LLC.
FDA 510(k) Regulatory Record - Curiteva, Inc.
11 devices
Cleared
Jan 16, 2026
Curiteva Porous PEEK Cervical Interbody System
Orthopedic
186d
Cleared
Jan 15, 2026
Curiteva Porous PEEK Cervical Interbody Fusion System
Orthopedic
29d
Cleared
Jun 18, 2025
Curiteva Porous PEEK Standalone ALIF System
Orthopedic
90d
Cleared
Oct 28, 2024
Curiteva Porous PEEK Laminoplasty System
Orthopedic
28d
Cleared
Feb 29, 2024
Curiteva Thoracolumbar Plate System
Orthopedic
153d
Cleared
Jan 18, 2024
Curiteva Porous PEEK Lumbar Interbody Fusion System
Orthopedic
57d
Cleared
Jun 28, 2023
Curiteva Laminoplasty System
Orthopedic
61d
Cleared
Feb 13, 2023
Curiteva Porous PEEK Cervical Interbody Fusion System
Orthopedic
510d
Cleared
Jan 06, 2023
Curiteva Navigation System
Orthopedic
85d
Cleared
Sep 09, 2021
Curiteva Sacroiliac Joint Fusion System
Orthopedic
211d
Cleared
Aug 28, 2019
Curiteva Pedicle Screw System
Orthopedic
54d