Deep Blue Medical Advances, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232924 | T-Line® Hernia Mesh | October 18, 2023 |
| K230227 | T-Line Hernia Mesh | February 23, 2023 |
| K221556 | T-Line Hernia Mesh | November 28, 2022 |
| K193144 | T-Line Hernia Mesh | March 30, 2020 |