A portable, electrically-powered device designed to emit blue light, red light, and infrared radiation (heating effect) for phototherapy treatment of mild skin disorders (e.g., mild acne), superficial skin wounds, musculoskeletal symptoms (e.g., pain, spasm, s
| Company | Devices | Share |
|---|---|---|
| Shenzhen Lescolton Medical Equipment Co.,Ltd. | 50 | 12% |
| Led Technologies Inc | 31 | 8% |
| Biophotas, Inc. | 29 | 7% |
| Shenzhen Rainbow Technology Co.,Ltd | 23 | 6% |
| Dongguan Hunter Electronic Technology Co., Ltd. | 20 | 5% |
| Guangdong Newdermo Biotech Co.,Ltd. | 19 | 5% |
| Platinum Led Holdings Llc | 16 | 4% |
| Shenzhen Yihong Lighting Co., Ltd. | 14 | 3% |
| Omm Imports Inc. | 11 | 3% |
| Shenzhen Ais Queen Medical Technology Co., Ltd. | 10 | 2% |
| Shenzhen Baria Technology Co.,Ltd | 9 | 2% |
| Shenzhen Kaiyan Medical Equipment Co,. Ltd | 9 | 2% |
Company = labeler of record on GUDID. 66 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 |
|---|---|---|
| ILY | Lamp, Infrared, Therapeutic Heating | 297 |
| OHS | Light Based Over The Counter Wrinkle Reduction | 207 |
| OLP | Over-The-Counter Powered Light Based Laser For Acne | 170 |
| GEX | Powered Laser Surgical Instrument | 19 |
| ILP | System, Communication, Non-Powered | 14 |
| NFO | Stimulator, Transcutaneous Electrical, Aesthetic Purposes | 11 |
Use these as the dimensions to specify in a tender line.
407 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Blue/red/infrared phototherapy lamp", from 66 companies. The largest labeler is Shenzhen Lescolton Medical Equipment Co.,Ltd. with 12% of records.
ILY (Lamp, Infrared, Therapeutic Heating), OHS (Light Based Over The Counter Wrinkle Reduction), OLP (Over-The-Counter Powered Light Based Laser For Acne), GEX (Powered Laser Surgical Instrument)
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.