Shenzhen Trious Medical Technology Co., 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 |
|---|
| K250448 | Disposable Percutaneous Nephrostomy Dilatation Kit | July 3, 2025 |
| K243830 | Disposable ureteral stent | May 14, 2025 |
| K243710 | Disposable ureteral access sheath | April 11, 2025 |