Data / Medical devices / China / Shenzhen Nuon Medical Equipment Co., Ltd.
Shenzhen Nuon Medical Equipment Co., Ltd.: FDA-registered device maker in ShenZhen Guangdong, China, 3 510(k) clearances
Shenzhen Nuon Medical Equipment Co., Ltd. is registered with the FDA (registration 3030541658) in ShenZhen Guangdong, China. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 12, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030541658
- Address
- 1F-3F, No.27-2, Xintang Rd, Xintian Comm, Fuhai Str, Baoan Dist, Shenzhen, Guangdong,China, ShenZhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Nuon Medical Equipment Co., Ltd. (10089959)
- Roles
- Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer
- First device listed
- January 26, 2024
- Registered through
- 2026
- Brand names listed
- EFFICACY BOOSTER, Mosquito Bite Healer, Mosquito Bite itch Healer, PlasmaGLO V-Lift EMS Mask(MK-23 ), Radiant Renewal Skincare Wand, Red Light Therapy Wand (HD-44D)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch | OSG | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 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 |
|---|---|---|---|---|---|---|
| October 12, 2025 | K251034 | Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) | NFO | Substantially Equivalent | Shenzhen Nuon Medical Equipment Co., Ltd. | accessdata.fda.gov |
| April 8, 2025 | K242151 | Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) | OHS | Substantially Equivalent | Shenzhen Nuon Medical Equipment Co., Ltd. | accessdata.fda.gov |
| December 19, 2024 | K242700 | Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-59C, HD-59D, HD-70, HD-72, HD-72A, HD-73A, HD-73B, HD-116, HD-116A, HD-53A, HD-53B) | OHS | Substantially Equivalent | Shenzhen Nuon Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- All makers of Pad, Heating, Powered
- All makers of Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch
Updated October 12, 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.