COMPANY

Centinel Spine

HQ: West Chester, PA source · centinelspine.com ↗ · Mid-Atlantic

Location: West Chester, PA · source · Oct 14, 2026

Profile checked Oct 10, 2026

Keywords: Symptomatic Cervical Disc Disease Degenerative Disc Disease Cervical Spine Degenerative Disease Cervical Spine Degenerative Disc Disease Grade 1 Spondylolisthesis Retrolisthesis Prodisc C Vivo STALIF®

3Trials (company is sponsor)2FDA records (2 yrs)

Timeline

Nov 1, 2025 Trial start —: Retrospective Analysis of Patients Implanted With 2 Levels of Prodisc® C Vivo Devices source ↗
Apr 25, 2025 FDA FDA 510(k) clearance: prodisc® L Instruments — K250554, Apr 25, 2025. Applicant at approval: Centinel Spine, LLC. source ↗
Dec 17, 2024 FDA FDA 510(k) clearance: prodisc® L Instruments — K242869, Dec 17, 2024. Applicant at approval: Centinel Spine, LLC. source ↗
Apr 24, 2023 Trial start —: Retrospective Study With Patients Treated With STALIF® C or M and Ti or FLX Implants for 1 and 2 Levels source ↗
Aug 5, 2019 Trial start Not phased (device or behavioral study): 2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C source ↗

Upcoming milestones

2030-12 (ESTIMATED) · · Retrospective Analysis of Patients Implanted With 2 Levels of Prodisc® C Vivo Devices · NCT07370493

Estimated primary completion per ClinicalTrials.gov. Dates move.

Clinical trials (lead sponsor) 3

Record	Title	Phase	Status	Start	Primary completion
NCT07370493	Retrospective Analysis of Patients Implanted With 2 Levels of Prodisc® C Vivo Devices	Not listed	Enrolling by invitation	Nov 1, 2025	2030-12 (estimated)
NCT04012996	2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C	Not phased (device or behavioral study)	Active, not recruiting	Aug 5, 2019	Aug 31, 2025 (estimated)
NCT05610397	Retrospective Study With Patients Treated With STALIF® C or M and Ti or FLX Implants for 1 and 2 Levels	Not listed	Unknown status (ClinicalTrials.gov)	Apr 24, 2023	Apr 30, 2024 (estimated)

FDA records (last 2 years)

Apr 25, 2025 FDA 510(k) clearance: prodisc® L Instruments — K250554, Apr 25, 2025. Applicant at approval: Centinel Spine, LLC. source ↗
Dec 17, 2024 FDA 510(k) clearance: prodisc® L Instruments — K242869, Dec 17, 2024. Applicant at approval: Centinel Spine, LLC. source ↗

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