Data / Medical devices / China / Ningbo Lecount Medical Technology Development Co., Ltd.
Ningbo Lecount Medical Technology Development Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance
Ningbo Lecount Medical Technology Development Co., Ltd. is registered with the FDA (registration 3011889389) in Ningbo Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 25, 2015. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3011889389
- Address
- 457 Longfei Road, Yunlong Industry Zone, Yingzhou District, Ningbo Zhejiang, China, 315135
- Owner or operator
- Ningbo Lecount Medical Technology Development Co., Ltd. (10050382)
- Roles
- Manufacturer
- First device listed
- November 10, 2015
- Registered through
- 2026
- Brand names listed
- Nuocande Plastic Manual Wheelchair Model NKD L07
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 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 25, 2015 | K151797 | Nuocande Plastic Manual Wheelchair Model NKD L07 | IOR | Substantially Equivalent | Ningbo Lecount Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 25, 2015. 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.