Data / Medical devices / China / Gu'an Yeolight Smart Electronics Co.,ltd
Gu'an Yeolight Smart Electronics Co.,ltd: FDA-registered device maker in Langfang Hebei, China, 1 510(k) clearance
Gu'an Yeolight Smart Electronics Co.,ltd is registered with the FDA (registration 3043177840) in Langfang Hebei, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 19, 2025. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3043177840
- Address
- Room 203 Building 1 beside No.12,Dongfang Street, High-Tech Zones, Gu'an, Langfang, Hebei Province, China, Langfang Hebei, China, 065500
- Owner or operator
- Gu'an Yeolight Smart Electronics Co.,Ltd (10094970)
- Roles
- Manufacturer
- First device listed
- January 11, 2026
- Registered through
- 2026
- Brand names listed
- IPL Hair Removal Device/SYL001AZ, SYL002AZ
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 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 |
|---|---|---|---|---|---|---|
| November 19, 2025 | K253035 | IPL Hair Removal Device (SYL001AZ, SYL002AZ) | OHT | Substantially Equivalent | Gu'An Yeolight Smart Electronics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated November 19, 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.