Data / Medical devices / China / Dongguan Miqiang Technology Co., Ltd
Dongguan Miqiang Technology Co., Ltd: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance
Dongguan Miqiang Technology Co., Ltd is registered with the FDA (registration 3019887520) in Dongguan Guangdong, China. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 15, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019887520
- Address
- Room 302, No.6, Gongye 4th Road, Hengjiangxia Village, Changping Town, Dongguan Guangdong, China, 523570
- Owner or operator
- Dongguan MiQiang Technology Co., Ltd (10082135)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 18, 2021
- Registered through
- 2026
- Brand names listed
- 360 degree high-frequency vibration rotating facial cleanser; XPRE429, SHIN100, Rotating facial cleanser; XPRE430, 3D light mask XPRE505, XPRE506, XPRE507, XPRE509, Light Therapy Device; Rechargeable Nail Lamp,XPRE123 XPRE062 XPRE063, ACCESSORY, SURGICAL APPAREL - Face Mask, ANYORK LED Light Therapy Masks, BE LUCENT STELLAR XPRE170 XPRE137 XPRE067; Heat Source For Bleaching Teeth Professional Light Teeth;, Blackhead Remover XPRE129 XPRE143 XPRE133; XPRE202, Blackhead Remover with LED Screen; XPRE441 Facial Acne Patch; XPRE508, Brush, Dermabrasion, Powered-Facial Cleansing; Brush:XPRE171; and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 15, 2026 | K261407 | XPREEN LED Light Therapy Masks (XPRE322, XPRE326, XPRE327, XPRE342, XPRE368, XPRE422, XPRE434, XPRE451, XPRE455, XPRE457, XPRE448, XPRE335, XPRE350, XPRE420, XPRE436, XPRE339, XPRE445) | OHS | Substantially Equivalent | Dongguan Miqiang Technology Co., Ltd. | accessdata.fda.gov |
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Updated July 15, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.