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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
- —
Catalogue (7907)
Page 5 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| AccuFit Lateral Plate System | 58-DA-0330 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPA-3214-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STC-2811 | FDA UDI | Class II | Active |
| Anterior Cervical Interbody Fusion Device | 45-TN-5012 | FDA UDI | Class I | Active |
| SureLOK MIS 3L | 63-ST-5045 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-PC2250-16 | FDA UDI | Class II | Active |
| Reform POCT System | 55-PM-4545 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STC-3216 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RD-0550 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPA-2208-2C | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TC-7570 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-LB-2060 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 10-P3915-17P | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-9500 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TP-5050 | FDA UDI | Class II | Active |
| Reform POCT System | 55-SC-0202 | FDA UDI | Class II | Active |
| MD-Max ULIF | 43-6100-080 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-RD-6708 | FDA UDI | Class I | Active |
| ShurFit MALIF System | 23-9013-02 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-TC-6535 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-TN-7410 | FDA UDI | Class I | Active |
| Reform Ti Modular | 39-MT-0401 | FDA UDI | Class II | Active |
| MD-Max ULIF | 43-7000-7545 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 00-901615-11 | FDA UDI | Class I | Active |
| Dakota ACDF System | 71-TN-0606 | FDA UDI | Class I | Active |
| Vault C ACDF System | 37-CP-4206 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BC-5560 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-EC1850-14 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-7550 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-MS-1012 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPA-3615-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPD-3215 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPB-2413-2C | FDA UDI | Class II | Active |
| Navigated Instrument System | 70-RF-0545 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-RL-0019 | FDA UDI | Class I | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-1070 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-SC-0501 | FDA UDI | Class II | Active |
| Reform Ti CT Modular MIS Pedicle Screw System | 64-PT-9590 | FDA UDI | Class II | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HTC-7570 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPA-2415-2C | FDA UDI | Class II | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-5525 | FDA UDI | Class II | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HT-9540 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTA-3206 | FDA UDI | Class II | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HT-1080 | FDA UDI | Class II | Active |
| Reform POCT System | 55-LT-5050 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-BK-0104 | FDA UDI | Class II | Active |
| Dakota ACDF System | 71-AL-6410 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 12-9002-15 | FDA UDI | Class I | Active |
| MD-Max ULIF | 43-7000-8570 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-TP-5545 | FDA UDI | Class II | Active |
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