Sunglor 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 |
| K253086 | LED Light Therapy Device (Models: SG-FM, SG-FE) | December 19, 2025 |
| K253073 | LED Light Therapy Device (SG-FSM, SG-NK, SG-CT) | November 19, 2025 |