Data / Medical devices / China / Shenzhen Shuge Medical Beauty Devices Co., Ltd.
Shenzhen Shuge Medical Beauty Devices Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Shuge Medical Beauty Devices Co., Ltd. is registered with the FDA (registration 3016994791) in Shenzhen Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 24, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3016994791
- Address
- 6th Floor, Building B, Jingang Science and Technology Park, Qiaotou Community, Fuhai Street, Baoan District, Shenzhen Guangdong, China, 518100
- Owner or operator
- shenzhen shuge medical beauty devices co., ltd. (10084860)
- Roles
- Manufacturer
- First device listed
- April 7, 2022
- Registered through
- 2026
- Brand names listed
- IPL hair removal, SG02, SJ01, SJ05, SJ08, SJ09, SJ15, SJ16 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 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 |
|---|---|---|---|---|---|---|
| April 24, 2024 | K240093 | IPL Home Use Hair Removal Device (SJ15) | OHT | Substantially Equivalent | Shenzhen Shuge Medical Beauty Devices Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Brush, Dermabrasion, Powered
- All makers of Massager, Therapeutic, Electric
Updated April 24, 2024. 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.