# Curiteva, Inc.

- Location (FDA's records): Tanner, AL
- FDA decisions: 15 (2018–2026): 15 510(k) clearances
- Names in FDA's records: Curiteva, Inc. (11); Curiteva, LLC (4)
- Product codes: ODP (4), KWQ (3), NQW (2), MAX (2), OLO (1), OUR (1), OVD (1), NKB (1)
- 510(k) review time since 2016: median 85 days, against 95 for FDA's reviews in the same codes and years (8 of 13 faster)
- Predicates its devices cite: 41 (9 its own); citations of its devices by later devices: 13 (9 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Globus Medical, Inc.: 3 (https://510kreport.com/company/globus-medical)
- Degen Medical: 3 (https://510kreport.com/company/degen-medical)
- Meditech Spine, LLC: 3 (https://510kreport.com/company/meditech-spine)
- Medtronic Sofamor Danek USA, Inc.: 3 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Titan Spine, LLC: 2 (https://510kreport.com/company/titan-spine)
- Genesys Spine: 2 (https://510kreport.com/company/genesys-spine)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Astura Medical: 1 (https://510kreport.com/company/astura-medical)

## Firms that cite its devices most
- Promethean Restorative, LLC: 1 (https://510kreport.com/company/promethean-restorative)
- Precision Spine, Inc.: 1 (https://510kreport.com/company/precision-spine)
- Nvision Biomedical Technologies, Inc.: 1 (https://510kreport.com/company/nvision-biomedical-technologies)
- NanoHive Medical, LLC: 1 (https://510kreport.com/company/nanohive-medical)

## Its most-cited devices
- K213030: Curiteva Porous PEEK Cervical Interbody Fusion System (2023), cited by 3
- K181589: Curiteva Lumbar Interbody Fusion System (2018), cited by 3
- K233744: Curiteva Porous PEEK Lumbar Interbody Fusion System (2024), cited by 2
- K181261: Curiteva Cervical Interbody Fusion System (2018), cited by 1
- K243137: Curiteva Porous PEEK Laminoplasty System (2024), cited by 1
- K210402: Curiteva Sacroiliac Joint Fusion System (2021), cited by 1

## Recent decisions
- K252205: Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System (Jan 16, 2026)
- K254061: Curiteva Porous PEEK Cervical Interbody Fusion System (Jan 15, 2026)
- K250845: Curiteva Porous PEEK Standalone ALIF System (Jun 18, 2025)
- K243137: Curiteva Porous PEEK Laminoplasty System (Oct 28, 2024)
- K233360: Curiteva Thoracolumbar Plate System (Feb 29, 2024)
- K233744: Curiteva Porous PEEK Lumbar Interbody Fusion System (Jan 18, 2024)
- K231232: Curiteva Laminoplasty System (Jun 28, 2023)
- K213030: Curiteva Porous PEEK Cervical Interbody Fusion System (Feb 13, 2023)

Source page: https://510kreport.com/company/curiteva