Data / Medical devices / China / Tianjin Promoting Medical Technology Co.,ltd
Tianjin Promoting Medical Technology Co.,ltd: FDA-registered device maker in Tianjin, China, 7 510(k) clearances
Tianjin Promoting Medical Technology Co.,ltd is registered with the FDA (registration 3022982004) in Tianjin, China. It lists 2 device types. The FDA files 7 510(k) clearances under its listings, the newest dated April 22, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3022982004
- Address
- Taihe Building, Xiyingmen Street, Xiqing District, Tianjin, China, 300000
- Owner or operator
- Tianjin Promoting Medical Technology Co.,Ltd (10093072)
- Roles
- Exporter to the US
- First device listed
- March 26, 2025
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair (n3901), Electric Wheelchair (w3902), Electric wheelchair (JJW-7002.JJW-7003), Power Wheelchair (jjw-6001), Scooter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Exporter to the US | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Exporter to the US | 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 22, 2026 | K260237 | Mobility Scooter (X-12, X-14, X-17) | INI | Substantially Equivalent | Wuyi Aichi Industry and Trade Co., Ltd. | accessdata.fda.gov |
| March 20, 2026 | K253849 | Electric wheelchair (JJW-7002, JJW-7003) | ITI | Substantially Equivalent | ZheJiang J&J Mobility Co., Ltd. | accessdata.fda.gov |
| May 7, 2025 | K242975 | Mobility Scooter (Model X-01, X-02) | INI | Substantially Equivalent | Wuyi Aichi Industry & Trade Co., Ltd. | accessdata.fda.gov |
| January 6, 2025 | K242139 | Mobility Scooter (YL-09B, YL-07) | INI | Substantially Equivalent | Yongkang Yile Vehicle Co., Ltd. | accessdata.fda.gov |
| October 8, 2024 | K240563 | Power Wheelchair (JJW-6001) | ITI | Substantially Equivalent | ZheJiang J&J Mobility Co., Ltd. | accessdata.fda.gov |
| September 5, 2024 | K241723 | Electric wheelchair (W3902) | ITI | Substantially Equivalent | Zhejiang Richall Medical Technology Co., Ltd. | accessdata.fda.gov |
| September 5, 2024 | K241721 | Electric wheelchair (N3901) | ITI | Substantially Equivalent | Zhejiang Richall Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated April 22, 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.