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 11 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SureLOK MIS 3L | 63-8700-04 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-TH-0451 | FDA UDI | Class II | Active |
| Slimplicity Anterior Cervical Plate System | 08-9026 | FDA UDI | Class I | Active |
| Interspinous Plate System | 29-FP-5045 | FDA UDI | Class II | Active |
| Reform POCT System | 55-PA-4026 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TC-9500 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-SK-8570 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TD-9590 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 10-P3215-19P | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-1017-35 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2810 | FDA UDI | Class II | Active |
| PSS System | SL1000 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-SK-9511 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STB-2214 | FDA UDI | Class II | Active |
| MD Vue Lateral Access | 54-SC-3000 | FDA UDI | N/A | Active |
| ShurFit Lumbar Interbody | 72-CPB-3209-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-3611 | FDA UDI | Class II | Active |
| Dakota ACDF System | 71-RS-0612 | FDA UDI | Class I | Active |
| Reform TI Pedicle Screw System | 39-SB-4530 | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-4020 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 21-1002 CA | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 00-901715-19 | FDA UDI | Class I | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-0040 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-EC1860-08 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BC-7545 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OPA-3212-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STC-2813 | FDA UDI | Class II | Active |
| Dakota ALIF System | 69-AM-2519 | FDA UDI | Class II | Active |
| Reform POCT System | 55-CH-0035 | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-BP-9560 | FDA UDI | Class II | Active |
| Accufit Lateral Plate System | 58-DA-0301 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-STD-2615 | FDA UDI | Class II | Active |
| Intervertebral Body Fusion Device | 50-0021 | FDA UDI | Class II | Active |
| MD-Vue™ Lateral Discectomy System | 60-BK-5000 | FDA UDI | Class II | Active |
| Reform MC HA Coated Pedicle Screw System | 59-HBC-1040 | FDA UDI | Class II | Active |
| Interbody Fusion | 1311TS | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-PC2460-12 | FDA UDI | Class II | Active |
| Reform Ti Modular HA Pedicle Screw System | 39-HM-7540 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-OTD-2813 | FDA UDI | Class II | Active |
| ShurFit® LLIF System | 23-PC2260-14 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 00-9003-09 | FDA UDI | Class I | Active |
| PSS System | SLP4540 | FDA UDI | Class II | Active |
| Sure-Lok Extended Tab Pedicle Screw System | 48-3000-6545 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2615-2C | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STC-2216 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TD-6540 | FDA UDI | Class II | Active |
| Reform POCT System | 55-IN-0713 | FDA UDI | Class I | Active |
| Reform HA Coated Pedicle Screw System | 39-PH-4530 | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-PC1855-10-2C | FDA UDI | Class II | Active |
| SureLOK Mini Posterior Cervical/Upper Thoracic System | 04-9083 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.