Curiteva, LLC
Curiteva, LLC appears in FDA public data with 0 recalls, 15 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 16, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K252205 | Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curite | January 16, 2026 |
| K254061 | Curiteva Porous PEEK Cervical Interbody Fusion System | January 15, 2026 |
| K250845 | Curiteva Porous PEEK Standalone ALIF System | June 18, 2025 |
| K243137 | Curiteva Porous PEEK Laminoplasty System | October 28, 2024 |
| K233360 | Curiteva Thoracolumbar Plate System | February 29, 2024 |
| K233744 | Curiteva Porous PEEK Lumbar Interbody Fusion System | January 18, 2024 |
| K231232 | Curiteva Laminoplasty System | June 28, 2023 |
| K213030 | Curiteva Porous PEEK Cervical Interbody Fusion System | February 13, 2023 |
| K223200 | Curiteva Navigation System | January 6, 2023 |
| K210402 | Curiteva Sacroiliac Joint Fusion System | September 9, 2021 |
| K191810 | Curiteva Pedicle Screw System | August 28, 2019 |
| K181589 | Curiteva Lumbar Interbody Fusion System | December 20, 2018 |
| K181549 | Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) | August 3, 2018 |
| K181562 | Curiteva Anterior Cervical Plate System | August 2, 2018 |
| K181261 | Curiteva Cervical Interbody Fusion System | July 9, 2018 |