Is this your brand? Sign in to claim ownership.
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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005739886
- DUNS Number
- —
Catalogue (7907)
Page 7 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sure-Lok Extended Tab Pedicle Screw System | 48-CU-55060 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-PC1855-10 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 10-C3915-15 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AG-1515-2C | FDA UDI | Class II | Unknown |
| ShurFit Lumbar Interbody | 72-OTA-3213 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-BK-0107 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STB-3209 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STD-2414 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-3609 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPD-3613 | FDA UDI | Class II | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBP-5560 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 49-DP-0013 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 21-1002-CA | FDA UDI | Class II | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-8550 | FDA UDI | Class II | Active |
| AccuFit Lateral Plate System | 58-BK-1001 | FDA UDI | Class II | Active |
| Reform Ti Modular | 73-MD-2800 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-SPC-2209 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-SC-0465 | FDA UDI | Class II | Active |
| Reform MC Screw System | 59-CP-0545 | FDA UDI | Class I | Active |
| Navigated Instrument System | 76-CR-0040 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TD-6525 | FDA UDI | Class II | Active |
| Reform MC Screw System | 59-LB-2100 | FDA UDI | Class I | Active |
| PSS System | SLP6545 | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | ACP235 | FDA UDI | Class II | Active |
| MD-Vue™ Lateral Discectomy System | 60-BK-5003 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPD-3611 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 50-0012 | FDA UDI | Class II | Active |
| NexGen Anterior Cervical Plate System | 65-DF-4010 | FDA UDI | Class II | Active |
| NexGen Anterior Cervical Plate System | 65-TF-4014 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 38-9212 | FDA UDI | Class I | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-7545 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPD-3214-2C | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-DA-1101 | FDA UDI | Class II | Active |
| Reform MC Screw System | 59-RD-0080 | FDA UDI | Class I | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9202 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 44-3015-12 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-CP-8512 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | TLIF24-12 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RP-9500 | FDA UDI | Class II | Active |
| MD-Max ULIF | 43-TL-8545 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-EC2255-16 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-SC-0100 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9009-35 | FDA UDI | Class I | Active |
| Anterior Cervical Interbody Fusion Device | 02-9001 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-STB-3013 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPD-3216-2C | FDA UDI | Class II | Active |
| Navigated Instrument System | 70-CT-1700 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-DA-1203 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTB-2815 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPC-2413 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.