Shenzhen Rogin Medical 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 |
|---|
| K242514 | Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO) | April 24, 2025 |
| K242383 | Apex Locator | March 7, 2025 |