Cathegenix (Xiamen) Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251469 | Endura Ureteral Stent and Stent Set | December 19, 2025 |
| K250585 | LumenaTM Ureteral Access Sheath | June 27, 2025 |