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Precision Spine, Inc.

Last updated September 17, 2026

What Precision Spine, Inc. makes

Precision Spine, Inc. manufactures spinal fixation hardware, including non-bioabsorbable bone screws, metallic and polymer-based interbody fusion cages, spinal plates, and internal fixation rods and connectors. Their portfolio also includes reusable orthopaedic surgical kits and composite spinal implants designed for anterior and posterior spinal procedures, such as cervical and lumbar fusions.

The company’s devices are classified under FDA’s Class I and Class II categories 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.

Information

Country: US
Address: 2050 Executive Dr, Pearl, MS, 39208
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005739886
DUNS Number: —

Catalogue (7907)

Page 12 of 159

Device	Model / Reference	Registries	Class	Status
Reform Ti Modular	39-TD-8511	FDA UDI	Class II	Active
MD Vue Lateral Access	54-BL-0120	FDA UDI	Class I	Active
Intervertebral Body Fusion Device	10-P3208-11P	FDA UDI	Class II	Active
SureLOK Mini Posterior Cervical/Upper Thoracic System	04-0500T	FDA UDI	Class II	Active
Anterior Cervical Interbody Fusion Device	50-0003	FDA UDI	Class II	Active
Reform Ti CT Modular MIS Pedicle Screw System	64-PM-9580	FDA UDI	Class II	Active
Intervertebral Body Fusion Device	ALN019	FDA UDI	Class I	Active
Vault C ACDF System	37-SC-0110	FDA UDI	Class II	Active
Interspinous Plate System	29-6000-CA	FDA UDI	Class II	Active
NexGen Anterior Cervical Plate System	65-BK-0102	FDA UDI	Class II	Active
Reform Ti Modular	39-TD-1060	FDA UDI	Class II	Active
Reform POCT System	55-IN-0066	FDA UDI	Class I	Active
Intervertebral Body Fusion Device	10-P3915-15P	FDA UDI	Class II	Active
ShurFit Lumbar Interbody	72-CPB-3207-2C	FDA UDI	Class II	Active
Reform POCT System	55-BK-0308	FDA UDI	Class II	Active
RCS Anterior Buttress Plate System	21-1050-CA	FDA UDI	Class II	Active
Reform Ti Modular	39-BK-0547	FDA UDI	Class II	Active
ShurFit Lumbar Interbody	72-STB-2614	FDA UDI	Class II	Active
Reform Ti Modular	39-TC-9550	FDA UDI	Class II	Active
Dakota ALIF System	69-RS-1513	FDA UDI	Class I	Active
ShurFit 2C Lumbar Interbody	23-PC2250-10-2C	FDA UDI	Class II	Active
Reform Midline Cortical Screw System	59-BP-5050	FDA UDI	Class II	Active
ShurFit Lumbar Interbody	72-SPB-2814	FDA UDI	Class II	Active
Reform TI Pedicle Screw System	39-SG-1045	FDA UDI	Class II	Active
Reform Midline Cortical Screw System	59-SC-5150	FDA UDI	Class II	Active
Interspinous Plate System	29-0610	FDA UDI	Class I	Active
ShurFit 2C Lumbar Interbody	23-EC2260-12-2C	FDA UDI	Class II	Active
Facet Screw System	35-S4535-K	FDA UDI	U	Active
ShurFit Interbody Device	44-3005-12	FDA UDI	Class II	Active
Reform TI Pedicle Screw System	39-TP-6540	FDA UDI	Class II	Active
Reform Pedicle Screw System	39-RP-5555	FDA UDI	Class II	Active
Reform Ti CT Modular MIS Pedicle Screw System	64-PM-8560	FDA UDI	Class II	Active
Reform Pedicle Screw System	39-ST-5200	FDA UDI	Class II	Active
Dakota ALIF System	69-AG-2015-2C	FDA UDI	Class II	Active
ShurFit Lumbar Interbody	72-TC-0607	FDA UDI	Class I	Active
SureLOK MIS 3L	63-9021	FDA UDI	Class I	Active
ShurFit Interbody System	ALIF36-17	FDA UDI	Class II	Active
ShurFit® LLIF System	23-PC2455-16	FDA UDI	Class II	Active
Reform Pedicle Screw System	39-SC-0103	FDA UDI	Class II	Active
Vault C ACDF System	37-TN-0408	FDA UDI	Class I	Active
ShurFit ACIF 2C	ACIF10-07P-2C	FDA UDI	Class II	Active
Dakota ALIF System	69-RM-2013	FDA UDI	Class I	Active
Reform MC HA Coated Pedicle Screw System	59-HBC-8550	FDA UDI	Class II	Active
ShurFit ACIF 2C	62-NR-5011	FDA UDI	Class I	Active
ShurFit Interbody Device	26-220800-13	FDA UDI	Class II	Active
Reform Pedicle Screw System	39-PA-9560	FDA UDI	Class II	Active
Reform Ti CT Modular MIS Pedicle Screw System	64-PT-8545	FDA UDI	Class II	Active
Reform POCT System	55-PM-4525	FDA UDI	Class II	Active
MD Vue Lateral Access	54-LC-5200	FDA UDI	Class I	Unknown
Dakota ALIF System	69-RM-0817	FDA UDI	Class I	Active

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