Ningbo Verykind Medical Device 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 |
|---|
| K211458 | Disposable Anorectal Staplers, Disposable Intraluminal Staplers, Disposable Linear Cutting Staplers, | December 30, 2021 |
| K202709 | Disposable Powered Endoscopic Linear Cutting Staplers and Cartridges | May 18, 2021 |