SHENZHEN SUPERLINE TECHNOLOGY 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 |
|---|
| K252223 | Alpha Endo Handpiece (Alpha Endo) | October 16, 2025 |
| K242765 | Electronic Apex Locator (Alpha Apex I) | January 17, 2025 |