Data / Medical devices / China / Guangzhou T&B Beauty Equipment Co., Ltd.
Guangzhou T&B Beauty Equipment Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 2 510(k) clearances
Guangzhou T&B Beauty Equipment Co., Ltd. is registered with the FDA (registration 3019705154) in Guangzhou Guangdong, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 25, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3019705154
- Address
- Room 201,No.83Building, Jiangxia East 1 road, Huangshi Street, Baiyun District, Guangzhou Guangdong, China, 510000
- Owner or operator
- GuangZhou T&B Beauty Equipment Co., Ltd. (10092059)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 29, 2024
- Registered through
- 2026
- Brand names listed
- AP02A, AP02B, AP02C, AP03A, AP03B, AP03C, AP05, AP07 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Marker, Skin | FZZ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 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 |
|---|---|---|---|---|---|---|
| September 25, 2024 | K241860 | Diode Laser Hair Removal System | GEX | Substantially Equivalent | Beijing Winkonlaser Technology Limited | accessdata.fda.gov |
| July 13, 1998 | K980040 | ELECTRONIC MUSCLE STIMULATOR - MICROSTIM J-1304D | IPF | Substantially Equivalent | Nisha Communication Industries | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Massager, Therapeutic, Electric
- All makers of Marker, Skin
- All makers of Stimulator, Muscle, Powered
Updated September 25, 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.