Data / Medical devices / China / Shenzhen JVK Medical Instruments Co.,ltd.
Shenzhen JVK Medical Instruments Co.,ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen JVK Medical Instruments Co.,ltd. is registered with the FDA (registration 3022594978) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 7, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3022594978
- Address
- Room 301,Building 2, No. 42, Fuyuan 1st Road, Heping Community, Fuhai Street, Baoan District, Shenzhen,Guangdo, Shenzhen Guangdong, China, 518000
- Owner or operator
- SHENZHEN JVK MEDICAL INSTRUMENTS CO.,LTD. (10084909)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 14, 2022
- Registered through
- 2026
- Brand names listed
- Hand-Held IPL Device(JOVS Graphene Hair Removal Device), Hand-held IPL device (JOVS Hair Removal Device), Multifunctional Beauty Mirror(JVK-703A)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| September 7, 2023 | K231800 | IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 | OHT | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Lamp, Infrared, Therapeutic Heating
Updated September 7, 2023. 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.