Data / Medical devices / China / Ningbo Dechang Electrical Machinery Made Co., Ltd.
Ningbo Dechang Electrical Machinery Made Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance
Ningbo Dechang Electrical Machinery Made Co., Ltd. is registered with the FDA (registration 3015603281) in Ningbo Zhejiang, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 4, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015603281
- Address
- 3rd Floor of 1# building of No. 18, No. 28 Yongxing East Road, Dongjiao Industrial Park, Yuyao, Ningbo Zhejiang, China, 315400
- Owner or operator
- Ningbo Dechang Electrical Machinery Made Co., Ltd. (10093559)
- Roles
- Manufacturer
- First device listed
- June 3, 2025
- Registered through
- 2026
- Brand names listed
- Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology model RT01
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 |
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 4, 2025 | K242068 | LED Light Therapy Mask (RT01) | OLP | Substantially Equivalent | Ningbo Dechang Electrical Machinery Made Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over The Counter Wrinkle Reduction
Updated April 4, 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.