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Shenzhen Fansizhe Science And Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K253881 | Intense Pulsed Light (IPL) System (Models: T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T | December 29, 2025 |
| K251173 | Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T | July 14, 2025 |
| K223928 | Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T0 | March 28, 2023 |
| K221569 | Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K | June 30, 2022 |
| K212881 | Intense Pulsed Light (IPL) System | April 11, 2022 |