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Sign in to claim this brandPrecision Spine, Inc.
US
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
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3005739886
- DUNS Number
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Catalogue (7907)
Page 15 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ShurFit 2C Lumbar Interbody | 23-EC2245-10-2C | FDA UDI | Class II | Active |
| PSS System | SLC6535 | FDA UDI | Class II | Active |
| MD Vue Discectomy | 60-BC-9188 | FDA UDI | Class I | Active |
| ShurFit MALIF System | 23-9011-02 | FDA UDI | Class I | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-6535 | FDA UDI | Class II | Active |
| Interbody Fusion | 11106PS | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | 08-4516f | FDA UDI | Class II | Active |
| Interspinous Plate System | 29-0128 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-IN-5100 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-SK-8560 | FDA UDI | Class II | Active |
| Reform Ti Modular HA Pedicle Screw System | 39-HM-4530 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9202-CA | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-SP-0555 | FDA UDI | Class I | Active |
| MD-Max ULIF | 43-2000-080 | FDA UDI | Class I | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-4545 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPB-2209-2C | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AS-2515 | FDA UDI | Class II | Active |
| Navigated Instrument System | 70-MC-0820 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPB-2613-2C | FDA UDI | Class II | Active |
| NexGen Anterior Cervical Plate System | 65-TF-4020 | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-MT-0403 | FDA UDI | Class II | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HT-8555 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-SC-0507 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STD-2411 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPD-2414-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPB-2815 | FDA UDI | Class II | Active |
| MD Vue Discectomy | 60-RD-7016 | FDA UDI | Class I | Active |
| Reform POCT System | 55-IN-0126 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-DS-9514 | FDA UDI | Class I | Active |
| Sure-Lok Extended Tab Pedicle Screw System | 48-CU-55040 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-LC-5120 | FDA UDI | Class II | Active |
| Facet Screw System | 35-S5040-X | FDA UDI | U | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-5555 | FDA UDI | Class II | Active |
| Anterior Cervical Interbody Fusion Device | 45-10-10P | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RU-5550 | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | 08-0112 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | PLIF25-13P-2C | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-SB-5025 | FDA UDI | Class II | Active |
| Reform POCT System | 55-IN-1406 | FDA UDI | Class I | Active |
| Anterior Cervical Interbody Fusion Device | 45-SC-0102 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-PC2250-14-2C | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 12-9013 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 10-IB30-17 | FDA UDI | Class I | Active |
| Slimplicity Plus Anterior Cervical Plating System | ACP126P | FDA UDI | Class II | Active |
| MD-Max ULIF | 43-7000-6535 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 26-250810-13 | FDA UDI | Class II | Active |
| PSS System | 100-5140 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-SC-5120 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-3207 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-EC1855-12-2C | FDA UDI | Class II | Active |
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