Data / Medical devices / China / Dongguan Yiyao Science & Technology Development Co., Ltd.
Dongguan Yiyao Science & Technology Development Co., Ltd.: FDA-registered device maker in Dongguan City Guangdong, China, 1 510(k) clearance
Dongguan Yiyao Science & Technology Development Co., Ltd. is registered with the FDA (registration 3038209294) in Dongguan City Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 3, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038209294
- Address
- Room501, NO. 11 Shennan yiheng street, Shenxiang, Qishi Town, Dongguan City Guangdong, China, 523000
- Owner or operator
- Dongguan Yiyao Science & Technology Development Co., Ltd. (10093234)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 16, 2025
- Registered through
- 2026
- Brand names listed
- Anti Snore Mouthpiece, Device, Anti-Snoring-BreazTek Anti Snore Mouthpiece, Kaitse ANTI SNORE MOUTHPIECE, Dental Orthodontic Retainer instruments (Positioner, Tooth, Preformed, Preformed tooth positione, Braces Orthodont,, Honpouyi Anti Snore Mouthpiece, Orthodontics, Dental Orthodontic Brackets, Dental Orthodontics, Dental Orthodontic Retainer instruments,, QuietLab Pro, orthodont dental, dental orthodont, orthodontic tools dental
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Positioner, Tooth, Preformed | KMY | 1 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| October 3, 2025 | K250028 | Anti Snore Mouthpiece | LRK | Substantially Equivalent | Dongguan Yiyao Science & Technology Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 3, 2025. 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.