Guilin Refine Medical Instrument Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K254018 | Portable Dental X-ray Device (GT-1) | February 19, 2026 |
| K230641 | Ultrasonic Scaler Tips | November 21, 2023 |
| K223414 | Curing Light, Model: MaxCure 9 | November 15, 2023 |