Data / Medical devices / China / Shanghai Hubang Intelligent Rehabilitation Equipment Co.,ltd
Shanghai Hubang Intelligent Rehabilitation Equipment Co.,ltd: FDA-registered device maker in Shanghai, China, 2 510(k) clearances
Shanghai Hubang Intelligent Rehabilitation Equipment Co.,ltd is registered with the FDA (registration 3030410174) in Shanghai, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 31, 2024. 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
- 3030410174
- Address
- Building 2, No.99, 819 Duhui Road, Minhang District, Shanghai, China, 201108
- Owner or operator
- Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd (10089708)
- Roles
- Manufacturer
- First device listed
- June 4, 2024
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair(HBLD3-B); Electric Wheelchair(HBLD3-E), Manual Wheelchair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 1 | Manufacturer | accessdata.fda.gov |
| 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 |
|---|---|---|---|---|---|---|
| May 31, 2024 | K240913 | Electric Wheelchair (HBLD3-B); Electric Wheelchair (HBLD3-E) | ITI | Substantially Equivalent | Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd | accessdata.fda.gov |
| December 12, 2008 | K083044 | HUBANG, MODEL HBL13/HBG12-S | IOR | Substantially Equivalent | Shanghai Hubang Medical Appliances Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 31, 2024. 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.