Data / Medical devices / China / Shenzhen Jian Feng Electronic Technology Co., Ltd
Shenzhen Jian Feng Electronic Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances
Shenzhen Jian Feng Electronic Technology Co., Ltd is registered with the FDA (registration 3009488655) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated May 9, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009488655
- Address
- #901,Block A, Fubilun Industrial Park,Chaoyang Rd Yanchuan Community,Yanluo Subdistrict,Bao an District, Shenzhen Guangdong, China, 518104
- Owner or operator
- Shenzhen Jian Feng Electronic Technology Co. Ltd (10042303)
- Roles
- Manufacturer
- First device listed
- May 26, 2021
- Registered through
- 2026
- Brand names listed
- AS1080,SM9126,FM-B2404,FM-B2409, FM-B2501, FM-B2503, FM-B2402, FM-B2403, TENS AND POWERED MUSCLE STIMULATOR: FM-B2403A,FM-B2405,Pro6ABS, TENS AND POWERED MUSCLE STIMULATOR: TU3424-F
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 |
|---|---|---|---|---|---|---|
| May 9, 2023 | K223825 | Tens & Ems Device | NUH | Substantially Equivalent | Shenzhen Jian Feng Electronic Technology Co., Ltd. | accessdata.fda.gov |
| March 8, 2022 | K213741 | TENS & EMS DEVICE (Model: FM-B2403A) | NUH | Substantially Equivalent | Shenzhen Jian Feng Electronic Technology Co., Ltd. | accessdata.fda.gov |
| March 3, 2022 | K213835 | TENS & EMS Device | NUH | Substantially Equivalent | Shenzhen Jian Feng Electronic Technology Co., Ltd. | accessdata.fda.gov |
| May 19, 2021 | K202866 | TENS & EMS Device | NUH | Substantially Equivalent | Shenzhen Jian Feng Electronic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated May 9, 2023. 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.