Data / Medical devices / China / Beijing Superlaser Technology Co., Ltd.
Beijing Superlaser Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 5 510(k) clearances
Beijing Superlaser Technology Co., Ltd. is registered with the FDA (registration 3017200975) in Beijing, China. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated September 3, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017200975
- Address
- Room101, 3rd floor, building3, Shengxiang street No.8 Daxing District, Beijing, China, 102600
- Owner or operator
- Beijing Superlaser Technology Co., Ltd. (10075781)
- Roles
- Manufacturer
- First device listed
- June 26, 2020
- Registered through
- 2026
- Brand names listed
- CO2 Laser System SL-COL402, CO2 Laser System SL-LC01, CO2 Laser System SL-LC02, Diode Laser 808nm SL-HR10, Diode laser therapy device VADER, Diode laser therapy device VADER-SL, Multi-modality workstation AAD Dual Light, Multi-modality workstation AAD Dual Light(SL-HV92) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 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 3, 2025 | K251457 | Diode laser therapy device (VADER) | GEX | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
| June 9, 2020 | K200042 | CO2 Laser System | GEX | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
| April 13, 2020 | K193464 | ND:YAG Laser | GEX | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
| December 10, 2019 | K192516 | Diode Laser 808nm | GEX | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
| November 27, 2019 | K192519 | Multi-modality workstation | ONF | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Updated September 3, 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.