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Curiteva, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252205Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; CuriteJanuary 16, 2026
K254061Curiteva Porous PEEK Cervical Interbody Fusion SystemJanuary 15, 2026
K250845Curiteva Porous PEEK Standalone ALIF SystemJune 18, 2025
K243137Curiteva Porous PEEK Laminoplasty SystemOctober 28, 2024
K233360Curiteva Thoracolumbar Plate SystemFebruary 29, 2024
K233744Curiteva Porous PEEK Lumbar Interbody Fusion SystemJanuary 18, 2024
K231232Curiteva Laminoplasty SystemJune 28, 2023
K213030Curiteva Porous PEEK Cervical Interbody Fusion SystemFebruary 13, 2023
K223200Curiteva Navigation SystemJanuary 6, 2023
K210402Curiteva Sacroiliac Joint Fusion SystemSeptember 9, 2021
K191810Curiteva Pedicle Screw SystemAugust 28, 2019
K181589Curiteva Lumbar Interbody Fusion SystemDecember 20, 2018
K181549Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System)August 3, 2018
K181562Curiteva Anterior Cervical Plate SystemAugust 2, 2018
K181261Curiteva Cervical Interbody Fusion SystemJuly 9, 2018