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 3 of 159| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Intervertebral Body Fusion Device | 38-9112 | FDA UDI | Class I | Active |
| ShurFit 2C Lumbar Interbody | 23-EC1850-14-2C | FDA UDI | Class II | Active |
| Interbody Fusion | 1131TS | FDA UDI | Class II | Active |
| Slimplicity Plus Anterior Cervical Plating System | 66-SV-4012 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPD-2413-2C | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-TC-1000 | FDA UDI | Class II | Active |
| Reform POCT System | 55-IN-2045 | FDA UDI | Class I | Active |
| MD Vue Lateral Access | 54-BP-0110 | FDA UDI | Class I | Active |
| MD Vue Discectomy | 60-RD-9012 | FDA UDI | Class I | Active |
| Vault C ACDF System | 37-TN-7806 | FDA UDI | Class I | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HT-1060 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STA-2609 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RD-0001 | FDA UDI | Class I | Active |
| Intervertebral Body Fusion Device | 10-4025 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-PA-1060 | FDA UDI | Class II | Active |
| Reform Ti Modular | 39-SK-4535 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-TP-9540 | FDA UDI | Class II | Active |
| PSS System | SLP6530 | FDA UDI | Class II | Active |
| Reform POCT System | 55-BK-0103 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-SG-1090 | FDA UDI | Class II | Active |
| Vault C ACDF System | 37-CL-4211 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-2416 | FDA UDI | Class II | Active |
| PSS System | SLPL6535 | FDA UDI | Class II | Active |
| Interspinous Plate System | 29-MP-5040 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | ALIF0832-13P | FDA UDI | Class II | Active |
| ShurFit 2C Lumbar Interbody | 23-EC2250-16-2C | FDA UDI | Class II | Active |
| Reform Midline Cortical Screw System | 59-LO-1220 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | 07-2915 | FDA UDI | Class II | Active |
| ShurFit Interbody Device | ALIF1526-19P | FDA UDI | Class II | Active |
| Reform POCT System | 55-PA-4516 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPC-3213-2C | FDA UDI | Class II | Active |
| NexGen Anterior Cervical Plate System | 65-TV-4010 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-MS-9560 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPA-3609 | FDA UDI | Class II | Active |
| Reform TI Pedicle Screw System | 39-HM-1050 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-STB-3012 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-SPA-2608-2C | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-BK-0800 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-RD-0030 | FDA UDI | Class I | Active |
| ShurFit Lumbar Interbody | 72-CPA-2814 | FDA UDI | Class II | Active |
| MD Vue Discectomy | 60-IN-9002 | FDA UDI | Class I | Active |
| Reform Ti HA Coated Pedicle Screw | 39-HTC-5555 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CTB-2807 | FDA UDI | Class II | Active |
| Reform Ti Modular | 63-SP-0720 | FDA UDI | Class I | Active |
| Anterior Cervical Interbody Fusion Device | ACIF05-11P | FDA UDI | Class II | Active |
| Dakota ACDF System | 71-AL-8508 | FDA UDI | Class II | Active |
| ShurFit MALIF System | 23-9013-06 | FDA UDI | Class I | Active |
| Vault C ACDF System | 37-SD-4017 | FDA UDI | Class II | Active |
| Reform Pedicle Screw System | 39-TH-0222 | FDA UDI | Class II | Active |
| ShurFit Lumbar Interbody | 72-CPC-3615 | 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.