# Dongguan Miqiang Technology Co., Ltd (contract manufacturer, Dongguan Guangdong, CN): 4 new FDA device listings, incl. accessory, surgical apparel

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Dongguan Miqiang Technology Co., Ltd |
| Owner / operator | Dongguan MiQiang Technology Co., Ltd |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device |
| Location | Dongguan Guangdong, CN |
| New listings | 4 |
| Devices | Accessory, Surgical Apparel; Over-The-Counter Powered Light Based Laser For Acne; Light Based Over The Counter Wrinkle Reduction; Toothbrush, Manual |
| Product codes | LYU, OLP, OHS, EFW |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Dental |
| Brand names | ACCESSORY, SURGICAL APPAREL - Face Mask; ANYORK LED Light Therapy Masks; Coolegend Led Light Therapy Masks (XPRE457); XPREEN LED Light Therapy Masks (XPRE322, XPRE326, XPRE327, XPRE342, XPRE368, XPRE422, XPRE434, XPRE451, XPRE455, XPRE457; SANATECH Led Light Therapy Mask (Mode: ORA Air); EZONA LED Light Therapy Mask, YULEOR LED Light Therapy Mask, RAYNOCTI LED Light Therapy Mask; ESTHELA Radiance A LED Light Therapy Mask: ESTHELA (XPRE451); Tigoola 2026 Upgraded Red Light Therapy Mask for Face with Near Infrared, 5 Modes - XPRE368 |
| First new listing | 2026-08-10 |
| Latest new listing | 2026-08-10 |
| FDA registration number | 3019887520 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.