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Centinel Spine, LLC

United States·US-MF-000013245

Last updated September 17, 2026

What Centinel Spine, LLC makes

Centinel Spine, LLC manufactures spinal fixation and replacement devices, including non-sterile bone-screw internal fixation systems for spinal stabilization, sterile and metal-polymer composite spinal fusion cages for interbody fusion, and modular cervical and lumbar total intervertebral disc prostheses for joint replacement.

The company’s products are classified as Class II and Class III devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Centinel Spine, LLC manufacture?

Centinel Spine, LLC specializes in spinal devices, including non-sterile bone-screw internal fixation systems for stabilizing the spine, sterile and metal-polymer composite spinal fusion cages for promoting bone growth between vertebrae, and modular cervical and lumbar total intervertebral disc prostheses designed to replace damaged spinal discs. These products address spinal stabilization, fusion, and joint replacement needs.

Where is Centinel Spine, LLC based?

The company is headquartered in the United States. This location aligns with regulatory frameworks governing medical device manufacturing and distribution in North America.

Which regulatory registries list Centinel Spine, LLC’s devices?

Centinel Spine’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify product details and compliance.

How are Centinel Spine, LLC’s devices classified under FDA regulations?

The company’s devices fall into two FDA classification categories: Class II and Class III. Class II devices generally pose moderate risk and require special controls beyond general controls, while Class III devices are higher risk and require pre-market approval due to insufficient data to ensure safety and effectiveness through other means.

What distinguishes Centinel Spine’s spinal fusion cages from other fixation systems?

Centinel Spine offers both sterile polymeric spinal fusion cages and metal-polymer composite cages, which combine materials to enhance structural support and bone integration. These are designed for interbody fusion, where cages are placed between vertebrae to promote healing, while their non-sterile bone-screw systems focus on direct spinal stabilization without fusion goals. The modular disc prostheses further extend functionality for joint replacement.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: Suite 3B, 900 Airport Road, PA, United States
Website: www.centinelspine.com/
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 0049 7333 925 99 80
PRRC Contact: Hoda El Outmani
EUDAMED SRN: US-MF-000013245
FDA FEI Number: 3007494564
DUNS Number: —

Catalogue (993)

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Device	Model / Reference	Registries	Class	Status
Pct	PCT0135027	FDA UDI	Class II	Active
Pct	PCT0440195	FDA UDI	Class II	Active
Stalif L	STL5540	FDA UDI	Class II	Active
Pct	PCT0140039	FDA UDI	Class II	Active
Pct	PCT0335125	FDA UDI	Class II	Active
Pct	PCT0440105	FDA UDI	Class II	Active
Pct	PCT0435175	FDA UDI	Class II	Active
Prodisc C Nova	PDNXLD6	FDA UDI	Class III	Active
Pct	PCT0145025	FDA UDI	Class II	Active
Pct	PCT0145045	FDA UDI	Class II	Active
Prodisc C	09.820.055S	FDA UDI	Class III	Active
Stalif C	C169579-3T	FDA UDI	Class II	Active
Midline Ii	M361520	FDA UDI	Class II	Active
Pct	PCT0440040	FDA UDI	Class II	Active
MIDLINE II-Ti	M331320c	FDA UDI	Class II	Active
Prodisc C Vivo	PDVMD7	FDA UDI	Class III	Active
Pct	PCT0335210	FDA UDI	Class II	Active
Pct	PCT0335230	FDA UDI	Class II	Active
Midline Ii	M301716	FDA UDI	Class II	Active
Pct	PCT0340145	FDA UDI	Class II	Active
Prodisc C Nova	PDNM7	FDA UDI	Class III	Active
Stalif Midline	STM6035R	FDA UDI	Class II	Active
Pct	PCT0235049	FDA UDI	Class II	Active
STALIF C-Ti	C141191-3Tc	FDA UDI	Class II	Active
Prodisc L	PDL-L-IP08S	FDA UDI	Class III	Active
Prodisc C Nova	PDNMD7	FDA UDI	Class III	Active
MIDLINE II-Ti	M392112c	FDA UDI	Class II	Active
Pct	PCT0340240	FDA UDI	Class II	Active
Stalif L	STL5512-10	FDA UDI	Class II	Active
Midline Ii	M391516	FDA UDI	Class II	Active
Pct	PCT0135023	FDA UDI	Class II	Active
STALIF C-Ti	C167559-3Dc	FDA UDI	Class II	Active
Pct	PCT0335095	FDA UDI	Class II	Active
STALIF C-Ti	C149581-3Dc	FDA UDI	Class II	Active
Pct	PCT0440075	FDA UDI	Class II	Active
Midline Ii	M421512	FDA UDI	Class II	Active
Prodisc C Nova	PDNXL7	FDA UDI	Class III	Active
Pct	PCT07LC013	FDA UDI	Class II	Active
Midline Ii	M391712	FDA UDI	Class II	Active
Pct	PCT0240035	FDA UDI	Class II	Active
Midline Ii	M331112	FDA UDI	Class II	Active
Pct	PCT0340130	FDA UDI	Class II	Active
Pct	PCT08FC027	FDA UDI	Class II	Active
Midline Ii	M422116	FDA UDI	Class II	Active
Pct	PCT0435115	FDA UDI	Class II	Active
Pct	PCT0335215	FDA UDI	Class II	Active
Pct	PCT0145041	FDA UDI	Class II	Active
MIDLINE II-Ti	M422108c	FDA UDI	Class II	Active
Midline Ii	M361912	FDA UDI	Class II	Active
Pct	PCT0245040	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

Emergo Europe B.V. NL

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (6)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Centinel Spine, LLC has six FDA recall records initiated between March 5, 2021, and March 20, 2026. The records include open, classified, and terminated statuses, with reasons involving product labeling errors—such as incorrect size labeling for the Prodisc C implants—and manufacturing issues, including missing markings on surgical components and potential foreign contamination in device inlays.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Mar 20, 2026	Z-2051-2026	—	open, classified	Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
Mar 20, 2026	Z-2050-2026	—	open, classified	Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
Dec 31, 2025	Z-1426-2026	—	open, classified	Products were mislabeled as the 6mm product but included the 5 mm product.
Jul 18, 2024	Z-3212-2024	—	open, classified	During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
Jul 18, 2024	Z-3213-2024	—	open, classified	During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
Mar 5, 2021	Z-1406-2021	—	terminated	Centinel Spine learned through five customer complaints that the product was missing the "UP" etching on the superior plate of the prodisc C device. Per the Surgical Technique, the "UP" is one of the methods used to indicate the direction in which the surgeon should place the prodisc C into intradiscal space. There are also "UP" indications in the packaging and on instrumentation as additional guides to help the surgeon properly implant the device that were present for the affected product.