Data / Medical devices / China / Shenzhen Goodwind Technology Development CO., LTD
Shenzhen Goodwind Technology Development CO., LTD: FDA-registered device maker in Shezhen Guangdong, China, 3 510(k) clearances
Shenzhen Goodwind Technology Development CO., LTD is registered with the FDA (registration 3010677917) in Shezhen Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 10, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010677917
- Address
- Room 801, Building 1, Baolong Intelligent Manufacturing Park, No. 34, Baotong Road, Baolong Community, Baolong Street, Longgang District, Shenzhen, P.R. China, Shezhen Guangdong, China, 518116
- Owner or operator
- Shenzhen Goodwind Technology Development CO., LTD (10046014)
- Roles
- Manufacturer
- First device listed
- January 23, 2014
- Registered through
- 2026
- Brand names listed
- DOUBLE INFRARED THERMAL THERAPY RED LIGHT THERMAL MASSAGER, Eye Recovery Pro (PH-e03), HEAT VIBRATION MASSAGER, HEAT VIBRATION REVIVING MASSAGER, Hand therapy device (Model:ph-h03), IPL Hair Removal Device (Model: ZHF-IPL-II, ZHF-IPL-III), Infrared Light Therapy Slippers (Model:ph-F01), Knee therapy device (Model:ph-k01) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | 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 |
|---|---|---|---|---|---|---|
| August 10, 2026 | K261602 | Eye Recovery Pro (PH-e03) | OHS | Substantially Equivalent | Shenzhen Goodwind Technology Development Co., Ltd. | accessdata.fda.gov |
| December 17, 2025 | K252983 | Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03) | OHS | Substantially Equivalent | Shenzhen Goodwind Technology Development Co., Ltd. | accessdata.fda.gov |
| September 28, 2022 | K222316 | IPL Hair Removal Device | OHT | Substantially Equivalent | Shenzhen Goodwind Technology Development 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
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Massager, Therapeutic, Electric
Updated August 10, 2026. 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.