Data / Medical devices / China / Huizhou C&D Industry Co., Ltd.
Huizhou C&D Industry Co., Ltd.: FDA-registered device maker in Huizhou Guangdong, China, 3 510(k) clearances
Huizhou C&D Industry Co., Ltd. is registered with the FDA (registration 3043749884) in Huizhou Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043749884
- Address
- Tangziling Section, Liantangmian Village, Sanhe Subdistrict, Huiyang District, Huizhou Guangdong, China, 516200
- Owner or operator
- Huizhou C&D Industry Co., Ltd. (10095242)
- Roles
- Foreign private label distributor, Repackager or relabeler
- First device listed
- February 10, 2026
- Registered through
- 2026
- Brand names listed
- IPL Hair Removal Device (CD-KA-M1, CD-KA-S1, CD-KA-D1), Micro-current Facial Beauty Device (CD-AM-810, CD-AM-812)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Foreign private label distributor, Repackager or relabeler | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Foreign private label distributor, Repackager or relabeler | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Foreign private label distributor, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Foreign private label distributor, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| November 14, 2025 | K252618 | IPL Hair Removal Device (I6 S1, I6 D1, I6 M1) | OHT | Substantially Equivalent | Alovea Healthcare Co. , Ltd. | accessdata.fda.gov |
| December 19, 2024 | K243430 | Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W) | NFO | Substantially Equivalent | Shenzhen Aozemei Technology Co., Ltd. | accessdata.fda.gov |
| October 28, 2024 | K241718 | Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W) | OHS | Substantially Equivalent | Shenzhen Aozemei Technology 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 Light Based Over-The-Counter Hair Removal
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Updated November 14, 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.