Celestray Biotech Company, LLC.,
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K230794 | Rebuilder Nerve Guidance Conduit | January 29, 2024 |
| K222220 | SpinMedix Absorbable Fibrous Membrane | July 6, 2023 |