Eden Spine Europe SA
Eden Spine Europe SA appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2072-2017, Class II) was initiated on March 17, 2017.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2072-2017 | Class II | GIZA Vertebral Body Replacement | March 17, 2017 |