Data / Medical devices / China / Ningbo Jindao Medical Device Technology Co.,ltd
Ningbo Jindao Medical Device Technology Co.,ltd: FDA-registered device maker in Ningbo Zhejiang, China, 3 510(k) clearances
Ningbo Jindao Medical Device Technology Co.,ltd is registered with the FDA (registration 3034732597) in Ningbo Zhejiang, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 27, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034732597
- Address
- 26# Tianjian Road, Ningbo Zhejiang, China, 315100
- Owner or operator
- Ningbo jindao medical device technology co.,ltd (10092223)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- December 15, 2024
- Registered through
- 2026
- Brand names listed
- Mobility Scooter (YL-09B, YL-07), Power Wheelchair (JJW-6001), Power wheelchair (ZS-EW8026)
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, 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 |
|---|---|---|---|---|---|---|
| March 27, 2026 | K254206 | Power wheelchair (ZS-EW8026) | ITI | Substantially Equivalent | Ningbo Zhishan Medical Technology 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 |
Compare with other makers
Updated March 27, 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.