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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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- —
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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 10 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Reform TI Pedicle Screw System | 39-SB-5555 | FDA UDI | Class II | Active |
| Reform POCT System | 55-IN-0110 | FDA UDI | Class I | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-0020 | FDA UDI | Class II | Active |
| Reform | 4773PS | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TC-7580 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-SP-0770 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPA-2606 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-BK-1025 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-1015-45 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AV-0813 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2214 | FDA UDI | Class II | Active |
| Reform Ti Modular HA Pedicle Screw System | 39-HM-5540 | FDA UDI | Class II | Active |
| Accufit Lateral Plate System | 58-PH-0100 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-SK-9560 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 26-220800-08 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-UP-7550 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-PA-9535 | FDA UDI | Class II | Active |
| PSS System | 63-CS-5530 | FDA UDI | Class II | Active |
| PSS System | SLC6560 | FDA UDI | Class II | Active |
| AccuFit RP System | RPIF13 | FDA UDI | Class II | Active |
| SureLOK MIS 3L | 63-ST-5500 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BC-5535 | FDA UDI | Class II | Active |
| SureLOK Pedicle Screw System | 09-9053 | FDA UDI | Class I | Active |
| Anterior Cervical Interbody Fusion Device | 45-TN-5008 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-MT-0402 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BC-8540 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-MS-8511 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-3616 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STD-2611 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-RB-2080 | FDA UDI | Class I | Active |
| ShurFit CRT Peek Cage | CRTP10-12 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AS-1519 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTD-2816 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TC-8580 | FDA UDI | Class II | Active |
| MD Vue Lateral Access | 54-RB-1000 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-SK-9590 | FDA UDI | Class II | Active |
| Reform POCT System | 55-IN-0550 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-OPB-2810 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-TH-0272 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-PA-5555 | FDA UDI | Class II | Active |
| Navigated Instrument System | 70-3L-0575 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPB-3211-2C | FDA UDI | Class II | Active |
| Reform POCT System | 55-BK-0312 | FDA UDI | Class II | Active |
| MD Vue Discectomy | 60-CH-0003 | FDA UDI | Class I | Active |
| Reform Pedicle Screw System | 39-SC-0505 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-EC2255-16-2C | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-SB-7555 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 07-2909 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RD-0415 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-OPA-2814 | FDA UDI | Class II | Active |
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