Data / Medical devices / China / Konliking Tech & Dev. Limited
Konliking Tech & Dev. Limited: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Konliking Tech & Dev. Limited is registered with the FDA (registration 3014159202) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 22, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014159202
- Address
- The 3nd Floor, Building 3, Floor 1/2/3, Building 2, Dawang Industrial Zone, Pinghu, Longgang, Shenzhen Guangdong, China, 518000
- Owner or operator
- KONLIKING TECH & DEV. LIMITED (10056347)
- Roles
- Manufacturer
- First device listed
- November 30, 2017
- Registered through
- 2026
- Brand names listed
- Air compression Therapy Device with models HW6007D, HW6007E-HW6007K;, Body massager, Neck shoulder massager, HW6007A Air Compression Therapy Device + Sleeve for Foot + Calf,, Electric Tooth brusher, Face Beauty Massager, Swing massager, Air massager, Pillow massager, Neck Massager, Cheek massager, Kneading massage,, Finger exerciser, Hand massager ball, Eyes Massager, 3D roller massager, Massager Cushion, Multifunction foot massager,, HW 6007C-H6007A, HW6007B;, HW01B Red light therapy waist belt, HW02 RED light therapy knee belt, HW03RED light therapy arm belt,, HW03A red light thearpy arm belt, HW05 Red light therapy belly belt, HW05A Red light therapy belly belt, and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Components, Exercise | IOD | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | 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 |
|---|---|---|---|---|---|---|
| February 22, 2021 | K210240 | Air Compression Therapy Device, model HW6007 | IRP | Substantially Equivalent | Konliking Tech & Dev. Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Massager, Powered Inflatable Tube
- All makers of Massager, Therapeutic, Manual
- All makers of Components, Exercise
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Toothbrush, Powered
Updated February 22, 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.