Data / Medical devices / China / Suzhou KD Intelligent Device Co., Ltd.
Suzhou KD Intelligent Device Co., Ltd.: FDA-registered device maker in TaiCang City Jiangsu, China, 1 510(k) clearance
Suzhou KD Intelligent Device Co., Ltd. is registered with the FDA (registration 3008466210) in TaiCang City Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 12, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008466210
- Address
- NO.36, GuGang Road, ChengXiang Town, TaiCang City Jiangsu, China, 215400
- Owner or operator
- SUZHOU KD INTELLIGENT DEVICE CO., LTD. (10032684)
- Roles
- Manufacturer
- First device listed
- November 17, 2025
- Registered through
- 2026
- Brand names listed
- Powered Wheelchair, PL001-9001
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| November 12, 2025 | K252829 | Powered Wheelchair (PL001-9001) | ITI | Substantially Equivalent | Suzhou KD Intelligent Device Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated November 12, 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.