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Zhejiang Chuangxiang Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K253132 | Single use stone retrieval balloons | March 6, 2026 |
| K251890 | Disposable Ureteral Stents | February 20, 2026 |
| K230773 | Endoscopy Irrigation Tubing | November 21, 2023 |
| K231471 | Air/Water Bottle Tubing, CO2 Source Tubing | September 8, 2023 |
| K220063 | Single Use Cytology Brush | July 28, 2022 |
| K212669 | Single Use Hemoclip | May 27, 2022 |
| K220065 | Single Use Ureteral Access Sheath | May 25, 2022 |
| K212668 | Sclerotherapy Needle | February 23, 2022 |
| K191900 | Single Use Grasping Forceps | March 27, 2020 |
| K192258 | Disposable Valve Sets | December 30, 2019 |
| K173758 | Disposable Biopsy Valve | May 14, 2018 |
| K172762 | Single Use Hemoclip | March 20, 2018 |
| K172758 | Rotatable Snares, Non-Rotatable Snares | March 7, 2018 |