Li Medical Corporation , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K252260 | RELIEEV HSG Catheter (HSG7FA1) | November 26, 2025 |
| K240364 | RELIEEV Uterine Manipulator Injector (CUMI 5.0) | October 16, 2024 |
| K240434 | RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) | September 25, 2024 |