Data / Medical devices / China / Beijing Honkon Technologies Co., Ltd.
Beijing Honkon Technologies Co., Ltd.: FDA-registered device maker in Beijing, China, 5 510(k) clearances
Beijing Honkon Technologies Co., Ltd. is registered with the FDA (registration 3009488834) in Beijing, China. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 2, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009488834
- Address
- No.72 building, No.16 Huanke Middle Rd Tongzhou District, Beijing, China, 100176
- Owner or operator
- Beijing Honkon Technologies Co., Ltd. (10045305)
- Roles
- Manufacturer
- First device listed
- November 4, 2013
- Registered through
- 2027
- Brand names listed
- 10600AH/10600AL/10600AL-30a/10600CH/10600CC/10600ZH/10600TH/10600KK/10600V01, 1064QCH/1064QCL/1064QEH/1064QCCH/1064QCCL/1064QKK/1064QPH/1064PVYL/1064PH03/1064QYD, 808CC/808KK/808CL/808CM/808CH/808EH/808BH/808DH/808AL/808CUTE/808VEH/808XF/808VEL/808FL/Superme ice-kk/808SS/808YK, S3C/S3D/M40e+/S1C+/S8C/S7C/M90e/M90e Plus, S3C/S3D/M40e+/S1C+/S8C/S7C/M90e/M90e Plus/DPL, SlimmingIII+,Slimming-VI,Slimming-VII,Slimming-448K,Slimming-v
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Vacuum, Light Induced Heating | NUV | 2 | Manufacturer | accessdata.fda.gov |
| 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 |
|---|---|---|---|---|---|---|
| March 2, 2017 | K161892 | Slimming Treatment Device | NUV | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
| April 24, 2014 | K131838 | DIODE LASER FOR HIAR REMOVAL | GEX | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
| January 22, 2014 | K131837 | CO2 FRACTIONAL LASER | GEX | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
| January 16, 2014 | K131857 | Q-SWITCHED ND:YAG LASER | GEX | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
| October 18, 2013 | K131859 | MULTIFUNCTIONAL SERIES | ONF | Substantially Equivalent | Beijing Honkon Technologies Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Massager, Therapeutic, Electric
- All makers of Massager, Vacuum, Light Induced Heating
- All makers of Powered Laser Surgical Instrument
Updated March 2, 2017. 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.