Data / Medical devices / China / Beijing Kes Biology Technology Co., Ltd.
Beijing Kes Biology Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 3 510(k) clearances
Beijing Kes Biology Technology Co., Ltd. is registered with the FDA (registration 3009444646) in Beijing, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 10, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009444646
- Address
- 101,1st Floor, underground 1-4 Floor,Building 3, No. 10, Linhe Street, Shunyi District, Beijing, China, 101300
- Owner or operator
- Beijing KES Biology Technology Co., Ltd. (10043218)
- Roles
- Manufacturer
- First device listed
- January 30, 2013
- Registered through
- 2026
- Brand names listed
- Diode Laser Therapy Systems, FUEsion IPLIQ, INTENSE PULSED LIGHT (IPL) SYSTEMS, MGD IPL BLACK, Nd YAG Laser Therapy Systems, Zemits EraseND, Zemits LightExpert
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 |
|---|---|---|---|---|---|---|
| May 10, 2021 | K210168 | Diode Laser Therapy Systems | GEX | Substantially Equivalent | Beijing Kes Biology Technology Co., Ltd. | accessdata.fda.gov |
| June 24, 2020 | K193477 | Nd: YAG Laser Therapy Systems | GEX | Substantially Equivalent | Beijing Kes Biology Technology Co., Ltd. | accessdata.fda.gov |
| January 22, 2013 | K122995 | INTENSE PULSED LIGHT (IPL) SYSTEMS | ONF | Substantially Equivalent | Beijing Kes Biology 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 May 10, 2021. 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.