Dio Medical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Known Names
dio medical, dio medical co
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223790 | Huvex Interspinous Fusion System | March 9, 2023 |
| K223140 | AEON-C Stand Alone System | December 20, 2022 |