A hand-held, electrically-powered device designed to be used in the home to produce strong, controlled flashes of filtered light in the wavelength range of 400 - 1200nm [intense pulsed light (IPL)] for self-removal of unwanted hair.
| Company | Devices | Share |
|---|---|---|
| Shenzhen Ulike Smart Electronics Co., Ltd. | 206 | 43% |
| Shenzhen Beauty Every Moment Intelligent Electric Co.,Ltd. | 41 | 9% |
| Dongguan Letme Medical Technology Co., Ltd. | 29 | 6% |
| Shenzhen Mlay Intelligent Technology Co., Ltd. | 27 | 6% |
| Shenzhen Fansizhe Science And Technology Co., Ltd. | 23 | 5% |
| Procter & Gamble Manufacturing Company, The | 21 | 4% |
| Shenzhen Semlamp Intelligent Technology Co., Ltd | 20 | 4% |
| Shenzhen Xiazhifeng Electronic Co., Ltd | 13 | 3% |
| Mustech Electronics Co., Limited | 12 | 3% |
| Shenzhen Jianchao Intelligent Technology Co., Ltd | 12 | 3% |
| Foshan Jindi Electric Appliance Co., Ltd. | 9 | 2% |
| Foreo Ab | 7 | 1% |
Company = labeler of record on GUDID. 31 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| OHT | Light Based Over-The-Counter Hair Removal | 480 |
| GEX | Powered Laser Surgical Instrument | 32 |
| OHT | Light based over-the-counter hair removal | 14 |
| ONF | Powered Light Based Non-Laser Surgical Instrument With Therm | 7 |
| OHS | Light Based Over The Counter Wrinkle Reduction | 2 |
Use these as the dimensions to specify in a tender line.
479 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Home-use intense pulsed light hair removal unit", from 31 companies. The largest labeler is Shenzhen Ulike Smart Electronics Co., Ltd. with 43% of records.
OHT (Light Based Over-The-Counter Hair Removal), GEX (Powered Laser Surgical Instrument), OHT (Light based over-the-counter hair removal), ONF (Powered Light Based Non-Laser Surgical Instrument With Therm)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.