Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF)
K251173 is the FDA 510(k) clearance record for Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF), a class II device, cleared for Shenzhen Fansizhe Science and Technology Co., Ltd. on under FDA product code OHT (Light Based Over-The-Counter Hair Removal). FDA's definition for product code OHT reads: "Over-the-counter device uses thermal energy to kill hair follicles for hair removal". FDA records list 5 510(k) clearances for Shenzhen Fansizhe Science and Technology Co., Ltd., from to . As of , FDA records show no recalls naming K251173.
Clearance record
- Decision date
- Received
- (89 days to decision)
- Product code
- OHT Light Based Over-The-Counter Hair Removal
- Regulation
- 21 CFR 878.4810
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Shenzhen Fansizhe Science and Technology Co., Ltd. 2nd, 3rd And 4th Floors, #11, Henggangxia Industrial Zone, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code OHT
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 3 |
| December 2025 | 2 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 3 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 2 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
