Data / Medical devices / China / Zhongshan Xiaolan Town Senlan Electronic Factory
Zhongshan Xiaolan Town Senlan Electronic Factory: FDA-registered device maker in Zhongshan City Guangdong, China, 1 510(k) clearance
Zhongshan Xiaolan Town Senlan Electronic Factory is registered with the FDA (registration 3016587556) in Zhongshan City Guangdong, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 8, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016587556
- Address
- 2/F, Plant 3, No.39 of Jucheng Avenue East, Xinshi Community, Xiaolan Town, Zhongshan City Guangdong, China, 528415
- Owner or operator
- Zhongshan XiaoLan Town SenLan Electronic Factory (10082358)
- Roles
- Manufacturer
- First device listed
- July 15, 2021
- Registered through
- 2026
- Brand names listed
- A-130B;A-208B;F-135B;F-136B;F-138TB;F-139B;F-998B;V-168B;K-100;K-108;K-200;K-208;K-300;K-303;F-16;F-28;V-68;V-99, A-209D, A-90; G5; G6, A1-D1, A1-D2, A2-DA, A2-D2, A2-D3, A3-G1T, A3-G2T, A6-G1T, A6-G2T, A6-G3T, A6-G, A2-D2/A6-G/A3-G1T/A6-G2/K-81/K-812/K-87, F-139/F-136/V-163/F-137/B-13/V-168/F-138/X-168/V-185/V-183/V-188B/V-263PB/F-998B/E-103/B-18/B-19/K-80/K-82/K-86/K-188/K-88/X-136, F-18/F-28/V-68/F-16/V-99/A-155/C-108/C-109/A-80/A-60/E-9/D-322/D-303/A-111/B-63/F-22/A-360/A-318/K-89/F-135B/A-208/V-168B/V-189B/A-130, Fetal Doppler, U8-25, U9-25 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | QUG | 2 | Manufacturer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Over The Counter | QUF | 1 | Manufacturer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Prescription | ESD | 1 | Manufacturer | accessdata.fda.gov |
| Monitor, Ultrasonic, Fetal | KNG | 2 | 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 |
|---|---|---|---|---|---|---|
| January 8, 2026 | K252669 | Fetal Doppler U8-25, U9-25 | KNG | Substantially Equivalent | Zhongshan Xiaolan Town Senlan Electronic Factory | accessdata.fda.gov |
Compare with other makers
- All makers of Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter
- All makers of Hearing Aid, Air-Conduction, Prescription
- All makers of Monitor, Ultrasonic, Fetal
- All makers of Hearing Aid, Air-Conduction, Over The Counter
Updated January 8, 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.