Daeju Meditech Engineering 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 |
|---|
| K242207 | NOABLE LASER | March 7, 2025 |
| K242206 | ACTIVO | September 27, 2024 |
| K211637 | AROMA GRAND | September 3, 2021 |