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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 8 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Reform Ti HA Coated Pedicle Screw | 39-HTC-7560 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPC-2815-2C | FDA UDI | Class II | Active |
| Reform MC Screw System | 59-RD-0200 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-STA-2816 | FDA UDI | Class II | Active |
| MD Vue Discectomy | 60-RD-4712 | FDA UDI | Class I | Active |
| ShurFit Interbody Device | 44-2505-12 | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | ACP-012 | FDA UDI | Class I | Active |
| Anterior Cervical Interbody Fusion Device | HTR-45-0005 | FDA UDI | Class I | Active |
| MD-Max ULIF | 43-TL-1090 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPB-3215 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-RD-0700 | FDA UDI | Class I | Active |
| Dakota ALIF System | 69-RG-1513 | FDA UDI | Class I | Active |
| Reform MC Screw System | 59-RB-1040 | FDA UDI | Class I | Active |
| ShurFit Interbody Device | PLIF22-14P | FDA UDI | Class II | Active |
| Reform Ti Modular HA Pedicle Screw System | 39-HMC-6545 | FDA UDI | Class II | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-5560 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTC-2416 | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-PM-5555 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AS-0819-2C | FDA UDI | Class II | Unknown |
| Dakota ACDF System | 71-TV-3515 | FDA UDI | Class II | Active |
| PSS System | 63-CS-8590 | FDA UDI | Class II | Active |
| Anterior Cervical Interbody Fusion Device | 21-1200-OC | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BC-1080 | FDA UDI | Class II | Active |
| SureLOK MIS 3L | 63-RD-9005 | FDA UDI | Class I | Active |
| Slimplicity Anterior Cervical Plate System | SDF4014 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-RG-1517 | FDA UDI | Class I | Active |
| SureLOK MIS 3L | 63-9038-24 | FDA UDI | Class I | Active |
| ShurFit Interbody Device | 26-221010-14 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | PLIF25-11P-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTC-3614 | FDA UDI | Class II | Active |
| MD-Vue™ Lateral Discectomy System | 60-BK-7005 | FDA UDI | Class II | Active |
| Reform POCT System | 55-SC-0302 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-SC-0201 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 10-C3215-13 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-RG-2017 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-DS-9511 | FDA UDI | Class I | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-7555 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AV-0815-2C | FDA UDI | Class II | Unknown |
| ShurFit Lumbar Interbody | 72-SPA-2815-2C | FDA UDI | Class II | Active |
| Navigated Instrument System | 70-MC-0555 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-PS-9515 | FDA UDI | Class I | Active |
| Reform POCT System | 55-BK-0101 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPA-2810 | FDA UDI | Class II | Active |
| Reform POCT System | 55-PM-3534 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-EC2255-14 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 12-9002-11 | FDA UDI | Class I | Active |
| Reform Midline Cortical Screw System | 59-BC-9500 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-RG-2013 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPA-2210-2C | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-RM-2019 | FDA UDI | Class I | Active |
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