Data / Medical devices / China / Foshan Zike Technology Co., Ltd.
Foshan Zike Technology Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance
Foshan Zike Technology Co., Ltd. is registered with the FDA (registration 3040278125) in Foshan Guangdong, China. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 6, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3040278125
- Address
- Room 503, 5th Floor, Workshop A, No. 5, Xiaheng 1st Road, Shayong, Lishui Town, Nanhai District, Foshan Guangdong, China, 528244
- Owner or operator
- Foshan Zike Technology Co., Ltd. (10094939)
- Roles
- Manufacturer
- First device listed
- January 7, 2026
- Registered through
- 2026
- Brand names listed
- 3D digital nail printer machine:ZK-P01,ZK-P02,ZK-P03,ZK-P04,ZK-P05,ZK-P06,, Air pressure suit:ZK-A01,ZK-A02,ZK-A03,ZK-A04,ZK-A05,ZK-A06,ZK-A07,ZK-A08,ZK-A09,ZK-A10,ZK-A11,ZK-A12,ZK-A13,, Body analyzer machine:ZK-BA01,ZK-BA02,ZK-BA03,ZK-BA04,ZK-BA05,ZK-BA06,ZK-BA07,ZK-BA08,ZK-BA09,, Diode Laser Hair Removal System:ZK-D01,ZK-D02,ZK-D03,ZK-D04,ZK-D05,ZK-D06,ZK-D07,ZK-D08,ZK-D09,ZK-D10,ZK-D11,ZK-D12,, Facial Spa Oxygen Hydro Facial Beauty System:ZK-F01,ZK-F02,ZK-F03,ZK-F04,ZK-F05,ZK-F06,, Fractional CO2 Laser System Machine:ZK-F01,ZK-F02,ZK-F03,ZK-F04,ZK-F05,ZK-F06,ZK-F07,, Hair Regrowth Machine:ZK-HG01,ZK-HG02,ZK-HG03,ZK-HG04,ZK-HG05,ZK-HG06,ZK-HG07,ZK-HG08,ZK-HG09,, Hyperbaric Oxygen Chamber:ZK-H01,ZK-H02,ZK-H03,ZK-H04,ZK-H05,ZK-H06, and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Calculator/Data Processing Module, For Clinical Use | JQP | 1 | Manufacturer | accessdata.fda.gov |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Manufacturer | accessdata.fda.gov |
| Gas, Laser Generating | NXF | 1 | Manufacturer | accessdata.fda.gov |
| Guide, Needle, Surgical | GDF | 1 | Manufacturer | accessdata.fda.gov |
| Marker, Skin | FZZ | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Syringe, Air And/Or Water | ECB | 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 |
|---|---|---|---|---|---|---|
| April 6, 2020 | K191970 | Diode Laser Hair Removal System | GEX | Substantially Equivalent | Beijing Sano Laser S&T Development Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Gas, Laser Generating
- All makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- All makers of Marker, Skin
- All makers of Guide, Needle, Surgical
- All makers of Calculator/Data Processing Module, For Clinical Use
- All makers of Pad, Heating, Powered
Updated April 6, 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.