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Beijing Keyi Medical Device Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K230120 | KeYi Total Knee System | April 19, 2024 |
| K191826 | KeYi Total Hip System | May 14, 2020 |
| K190567 | KeYi Spinal Fixation System | May 8, 2019 |
| K162380 | Locking Plate System | May 2, 2017 |