Data / Medical devices / China / Beijing Nubway S&T Co.,Ltd.
Beijing Nubway S&T Co.,Ltd.: FDA-registered device maker in Beijing, China, 8 510(k) clearances
Beijing Nubway S&T Co.,Ltd. is registered with the FDA (registration 3017124433) in Beijing, China. It lists 5 device types. The FDA files 8 510(k) clearances under its listings, the newest dated September 17, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017124433
- Address
- 202, No.5 workshop, No.1 caida 3rd Road Nancai Shunyi District, Beijing China, Beijing, China, 101300
- Owner or operator
- Beijing Nubway S&T Co.,Ltd. (10074939)
- Roles
- Manufacturer
- First device listed
- June 8, 2020
- Registered through
- 2026
- Brand names listed
- Diode Laser Hair Removal Machine QDTM-01, Diode laser hair removal machine (QDTM-04), Diode laser hair removal machine QDTM-02, Electromagnetic Stimulator Device-QEZJ-01, LED Therapy Device (QLXY-01), LED Therapy Device-QLXY-01, Q Switched Nd: YAG Laser machine QLHF-02, Q Switched Nd:YAG Laser machine (QLQW-01) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gas, Laser Generating | NXF | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light, Surgical, Accessories | FTA | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 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 17, 2026 | K261673 | LED Therapy Device (QLXY-01) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| August 11, 2026 | K261841 | Q Switched Nd:YAG Laser machine (QLQW-01) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| July 17, 2026 | K261693 | Diode laser hair removal machine (QDTM-04) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| July 16, 2026 | K261674 | Skin Air Cooling System (QALF-01) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| April 28, 2025 | K242951 | Diode laser hair removal machine (QDTM-02) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| March 3, 2025 | K242943 | Q Switched Nd:YAG Laser machine (QNHF-01) | GEX | Substantially Equivalent | Beijing Nubway S&T Co., Ltd. | accessdata.fda.gov |
| April 3, 2020 | K192735 | Diode Laser Hair Removal Machine | GEX | Substantially Equivalent | Beijing Lead Beauty S & T Co., Ltd. | accessdata.fda.gov |
| March 20, 2020 | K193609 | Q Switched Nd: YAG Laser machine | GEX | Substantially Equivalent | Beijing Lead Beauty S & T Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light, Surgical, Accessories
- All makers of Massager, Therapeutic, Electric
- All makers of Powered Laser Surgical Instrument
- All makers of Gas, Laser Generating
- All makers of Lamp, Infrared, Therapeutic Heating
Updated September 17, 2026. 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.