Data / Medical devices / China / Shenzhen Qianyu Technology Co., Ltd.
Shenzhen Qianyu Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 5 510(k) clearances
Shenzhen Qianyu Technology Co., Ltd. is registered with the FDA (registration 3019577501) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 17, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019577501
- Address
- Room 301,Building 2, No. 42, Fuyuan 1st Road, Heping Community, Fuhai Street, Baoan District, Shenzhen,Guangdo, Shenzhen Guangdong, China, 518103
- Owner or operator
- Shenzhen Qianyu Technology Co., Ltd. (10084911)
- Roles
- Exporter to the US, Specification developer
- 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), JOVS CoreEnergy EMS body Shaping led light Therapy Belt (JQ21), JOVS EMS 6D FOCUS MASK (JM2X), JOVS EMS-Toning Shorts(JW1,JW1P,JW1X), JOVS Electric Stimulation Beauty Device (JE2), JOVS HLLT Hair Density Dryer (JN5), JOVS LED Neck & Chest Mask(JNL1) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Specification developer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Exporter to the US, Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Specification developer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 17, 2025 | K250227 | JOVS Electric Stimulation Beauty Device (JE2) | NFO | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
| May 1, 2025 | K244020 | Wrinkle Treatment Device (JM1, JM2B) | OHS | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
| April 5, 2024 | K240360 | Wrinkle Treatment Device (JM2) | OHS | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
| April 27, 2022 | K220645 | Hand-held IPL device (JOVS Hair Removal Device) | OHT | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
| March 28, 2022 | K214113 | Hand-held IPL device(JOVS Graphene Hair Removal Device) | OHT | Substantially Equivalent | Shenzhen Qianyu Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Tape And Bandage, Adhesive
- All makers of Massager, Therapeutic, Electric
Updated October 17, 2025. 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.