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Sign in to claim this brandPrecision Spine, Inc.
US
Last updated September 17, 2026
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 9 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ShurFit Lumbar Interbody | 72-OPC-2413-2C | FDA UDI | Class II | Active |
| Reform POCT System | 55-PM-4535 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-BK-0307 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RD-0032 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-TS-7208 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 00-901715-13 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-DC-9512 | FDA UDI | Class I | Active |
| Reform POCT System | 55-PM-3538 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 26-251005-12 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RP-9560 | FDA UDI | Class II | Active |
| Interspinous Plate System | 29-1000 | FDA UDI | Class I | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-1012 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-TR-1050 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2609 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-3010 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-SB-4022 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | ALIF1532-15P | FDA UDI | Class II | Active |
| Facet Screw System | 35-S5030-X | FDA UDI | U | Active |
| Interbody Fusion Devices | 11105PS | FDA UDI | Class II | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-5530 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9004 | FDA UDI | Class I | Active |
| ShurFit MALIF System | 23-9041 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | ALN004 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 00-9005-10 | FDA UDI | Class I | Active |
| NexGen Anterior Cervical Plate System | 65-TV-4510 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTA-3211 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-MS-4530 | FDA UDI | Class II | Active |
| Reform POCT System | 55-PB-4022 | FDA UDI | Class II | Active |
| Reform POCT System | 55-LS-0100 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | ALIF1532-19P | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | SDF4012-B | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-TR-1040 | FDA UDI | Class II | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-7535 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | PLIF22-13P-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPD-2215 | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-PT-8555 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AG-2515-2C | FDA UDI | Class II | Unknown |
| ShurFit Lumbar Interbody | 72-SPA-2215-2C | FDA UDI | Class II | Active |
| Anterior Cervical Interbody Fusion Device | 50-0022 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-TR-8500 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-DS-9514 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPB-3210-2C | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-PM-4530 | FDA UDI | Class II | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-5540 | FDA UDI | Class II | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HTC-9540 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPB-2816-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPB-2214 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BK-0505 | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-RD-0411 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-BK-0151 | FDA UDI | Class II | Active |
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