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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 2 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ShurFit Lumbar Interbody | 72-CH-0002 | FDA UDI | Class I | Active |
| Reform POCT System | 55-PM-3526 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-1055 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-PC1855-08-2C | FDA UDI | Class II | Active |
| AccuFit ALIF Plate System | 01-F5535 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-LT-5120 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-CL-8511 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 26-251005-13 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTB-2415 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BK-0475 | FDA UDI | Class II | Active |
| MD Vue Lateral Access | 54-DH-0001 | FDA UDI | Class I | Active |
| Reform Ti Modular HA Pedicle Screw System | 39-HM-7550 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AV-0815 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-3210 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 38-2915 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TD-7530 | FDA UDI | Class II | Active |
| PSS System | 63-CR-5535 | FDA UDI | Class II | Active |
| PSS System | SLP6525 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 10-S3215-11 | FDA UDI | Class I | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9032 | FDA UDI | Class I | Active |
| Reform Midline Cortical Screw System | 59-SC-5200 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-5040 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-BK-0600 | FDA UDI | Class II | Active |
| Reform POCT System | 55-PM-3508 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AG-2017 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPC-3215 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AV-2515 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-MU-4535 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AG-3017 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STC-3016 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STA-2607 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-4030 | FDA UDI | Class II | Active |
| Reform | 5252PS | FDA UDI | Class II | Active |
| ShurFit Interbody Device | ALIF0839-13P | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-SP-0760 | FDA UDI | Class I | Active |
| Reform TI Pedicle Screw System | 39-BK-0704 | FDA UDI | Class II | Active |
| PSS System | 100-5110 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | TLIF30-08P-2C | FDA UDI | Class II | Active |
| Dakota ACDF System | 71-IN-0315 | FDA UDI | Class I | Active |
| Reform Pedicle Screw System | 39-LT-5060 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TR-5055 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-PC2260-08-2C | FDA UDI | Class II | Active |
| MD-Max ULIF | 43-7000-5540 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 00-9005-08 | FDA UDI | Class I | Active |
| MD-Max ULIF | 43-TL-5560 | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | SDV4518-B | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-SC-1608 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-8560 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPB-2408 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2413 | FDA UDI | Class II | Active |
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