Data / Medical devices / China / Beijing Goldenlaser Development Co., Ltd.
Beijing Goldenlaser Development Co., Ltd.: FDA-registered device maker in Beijing, China, 3 510(k) clearances
Beijing Goldenlaser Development Co., Ltd. is registered with the FDA (registration 3009078366) in Beijing, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 31, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009078366
- Address
- A2-53A, No. 65 South Third Ring West Road Fengtai District, Beijing, China, 100069
- Owner or operator
- Beijing Goldenlaser Development Co., Ltd. (10087156)
- Roles
- Manufacturer
- First device listed
- January 19, 2023
- Registered through
- 2026
- Brand names listed
- CO2 FRACTIONAL LASER MACHINE: GL005, GL006, GL012, GL061, GL063, CO2 Laser System:GL060, GL062, GL065, GL066, GL067, GL068, COOLING DIODE LASER MACHINE: GLD12, GLD13, GLD15, CRYO SLIMMING MACHINE: GLV1, GLV2, GLV3, GLV5, GLV6, GLV8, GLV9, GLV10, DIODE LASER MACHINE: DLT05, DLT06, GLT07, GLT08, DIODE LASER MACHINE: GLD02, GLD03, GLD05, GLD06, GLD07, GLD08, GLD09, GLD11, GLD18, GLD19, GLD22, GLD23, Diode Laser Hair removal Machine: GLD01, GLD10, GLD16,GLD19, ERBIUM LASER MACHINE: GLC01, GLC02, GLC03, GLC05 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gas, Laser Generating | NXF | 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 |
|---|---|---|---|---|---|---|
| March 31, 2026 | K260375 | Nd: YAG Laser Therapy Systems | GEX | Substantially Equivalent | Sanhe Meditech Co., Ltd. | accessdata.fda.gov |
| March 28, 2026 | K260257 | CO2 Laser System | GEX | Substantially Equivalent | Sanhe Meditech Co., Ltd. | accessdata.fda.gov |
| October 31, 2025 | K252427 | Diode Laser Hair Removal Machine (GLD01) | GEX | Substantially Equivalent | Sanhe Meditech Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 31, 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.