COMPANY

Curiteva

Location: Tanner, AL · source · Oct 15, 2026

Profile checked Oct 10, 2026

Timeline

Jan 16, 2026 FDA FDA 510(k) clearance: Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF Syste source ↗
Jan 15, 2026 FDA FDA 510(k) clearance: Curiteva Porous PEEK Cervical Interbody Fusion System — K254061, Jan 15, 2026. Applicant at approval: Curiteva, Inc. source ↗
Jun 18, 2025 FDA FDA 510(k) clearance: Curiteva Porous PEEK Standalone ALIF System — K250845, Jun 18, 2025. Applicant at approval: Curiteva, Inc. source ↗
Oct 28, 2024 FDA FDA 510(k) clearance: Curiteva Porous PEEK Laminoplasty System — K243137, Oct 28, 2024. Applicant at approval: Curiteva, Inc. source ↗

Jan 16, 2026 FDA 510(k) clearance: Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System — K252205, Jan 16, 2026. Applicant at approval: Curiteva, Inc. source ↗
Jan 15, 2026 FDA 510(k) clearance: Curiteva Porous PEEK Cervical Interbody Fusion System — K254061, Jan 15, 2026. Applicant at approval: Curiteva, Inc. source ↗
Jun 18, 2025 FDA 510(k) clearance: Curiteva Porous PEEK Standalone ALIF System — K250845, Jun 18, 2025. Applicant at approval: Curiteva, Inc. source ↗
Oct 28, 2024 FDA 510(k) clearance: Curiteva Porous PEEK Laminoplasty System — K243137, Oct 28, 2024. Applicant at approval: Curiteva, Inc. source ↗

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