Data / Medical devices / China / Guangzhou Amili Beauty Technology Co., Ltd.
Guangzhou Amili Beauty Technology Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 1 510(k) clearance
Guangzhou Amili Beauty Technology Co., Ltd. is registered with the FDA (registration 3039080630) in Guangzhou Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 14, 2011. 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
- 3039080630
- Address
- Room 613, 6th Floor, Building 902 Xingnan Avenue, Nancun Town, Guangzhou, Guangdong, Guangzhou Guangdong, China, 511442
- Owner or operator
- Guangzhou Amili Beauty Technology Co., Ltd. (10094435)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer
- First device listed
- November 29, 2025
- Registered through
- 2026
- Brand names listed
- Cryo fat freeziong slimming machine, EM Slim body Sculpting Beauty Machine, EMS Belt, EMS Slimming Machine, Facial cleansing machine, Fat freezing machine, Fractional CO2 laser machine, GEX - Powered laser surgical instrument and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Contract manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Remanufacturer | 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 14, 2011 | K103501 | ALMA LASERS PIXEL CO2 LASER SYSTEM, DELIVERY DEVICE AND ACCESSORIES | GEX | Substantially Equivalent | Alma Lasers, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Powered Laser Surgical Instrument
- All makers of Massager, Therapeutic, Electric
Updated January 14, 2011. 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.