IPL Hair Removal Device (model: KCA450, KCA446, KCA504, KCA505, KCA506, KCA507, KCA508, KCA509, KCA501, KCA423, KCA448, KCA449, KCA502, KCA521)
K240282 is the FDA 510(k) clearance record for IPL Hair Removal Device (model: KCA450, KCA446, KCA504, KCA505, KCA506, KCA507, KCA508, KCA509, KCA501, KCA423, KCA448, KCA449, KCA502, KCA521), a class II device, cleared for Dongguan Boyuan Intelligent 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 4 510(k) clearances for Dongguan Boyuan Intelligent Technology Co.,Ltd, from to . As of , FDA records show no recalls naming K240282.
Clearance record
- Decision date
- Received
- (62 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
- Dongguan Boyuan Intelligent Technology Co.,Ltd Rm. 801, Bldg. 3, #3 Kuiqiao Rd.,, Dongguan, CN
- 510(k) summary
- Statement
- 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 |
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