Data / Medical devices / China / Shenzhen Qiaochengli Technology Co., Ltd
Shenzhen Qiaochengli Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Qiaochengli Technology Co., Ltd is registered with the FDA (registration 3018366453) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018366453
- Address
- Room 1220, Block A, Bairuida Building, Banxuegang Avenue, Vanke City Community, Bantian Subdistrict, Longgang, Shenzhen Guangdong, China, 518100
- Owner or operator
- Shenzhen Qiaochengli Technology Co., Ltd (10080983)
- Roles
- Specification developer
- First device listed
- March 17, 2026
- Registered through
- 2026
- Brand names listed
- FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S), IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S,
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Specification developer | 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 14, 2025 | K252234 | IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S) | OHT | Substantially Equivalent | Shenzhen Qiaochengli Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 14, 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.