Data / Medical devices / China / Beijing Mingqiao Technology Co., Ltd.
Beijing Mingqiao Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 4 510(k) clearances
Beijing Mingqiao Technology Co., Ltd. is registered with the FDA (registration 3033884002) in Beijing, China. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 9, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033884002
- Address
- Pilot Free Trade Zone, No. 3813, Block D, 12 Yushun Road, Daxing District, China, Beijing, China, 100026
- Owner or operator
- Beijing Mingqiao Technology Co., Ltd. (10091842)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 7, 2024
- Registered through
- 2026
- Brand names listed
- CO2 Laser System - COL408, CO2 Laser System - CRL308, CO2 Laser System - SL-LC01, Diode Laser 808nm - DLV545, Diode Laser 808nm - DLV548, Diode Laser 808nm - DLV549, Diode Laser 808nm - DLV557, Diode Laser 808nm - DLV603 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| 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 June 9, 2020. 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.