Eminent Spine
Eminent Spine appears in FDA public data with 0 recalls, 15 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on October 7, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 4
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250894 | Eminent Spine Posterior SI System | October 7, 2025 |
| K241663 | Eminent Spine 3D Titanium Pedicle Screw System | April 28, 2025 |
| K242069 | Eminent Spine Scoliosis Deformity Pedicle Screw System | September 3, 2024 |
| K240505 | Eminent Spine SI Screw System | June 4, 2024 |
| K230219 | Eminent Spine 3D Lumbar Interbody Fusion Systems | May 16, 2023 |
| K212701 | Eminent Spine 3D Cervical Interbody Fusion System | February 6, 2023 |
| K221936 | Standalone ALIF Interbody Fusion System | October 17, 2022 |
| K212853 | Cervical Stand-Alone System | November 5, 2021 |
| K201979 | Cervical Plate System | August 25, 2020 |
| K143365 | Eminent Foot Plate System | March 30, 2015 |
| K133194 | DIAMOND RATTLESNAKE SYSTEM | June 26, 2014 |
| K103068 | KING COBRA ANTERIOR CERVICAL PLATE | January 14, 2011 |
| K100377 | DIAMONDBACK SPINAL SYSTEM | April 22, 2010 |
| K090415 | EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEM | June 1, 2009 |
| K090064 | EMINENT SPINE INTERBODY FUSION SYSTEM | April 9, 2009 |