Data / Medical devices / China / Jiangsu Bangbang Intelligent Technology Co., Ltd.
Jiangsu Bangbang Intelligent Technology Co., Ltd.: FDA-registered device maker in Changzhou City Jiangsu, China, 1 510(k) clearance
Jiangsu Bangbang Intelligent Technology Co., Ltd. is registered with the FDA (registration 3030671633) in Changzhou City Jiangsu, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 30, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030671633
- Address
- Building 1, No.2 Hongren Road, Tianning District, Changzhou City Jiangsu, China, 213000
- Owner or operator
- Jiangsu Bangbang Intelligent Technology Co., Ltd. (10090131)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- February 19, 2024
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair (Robooter E60), Electric Wheelchair (Robooter E80)(BBR-E80-01), Electric Wheelchair (Robooter E80) (BBR.E80-02), Electric wheelchair, Electric wheelchair (Robooter E40), Mobility Scooter (BBR-Q40-01); Mobility Scooter (BBR-Q40-02); Mobility Scooter (BBR-Q40-03);, Mobility Scooter (BBR-Q40-04); Mobility Scooter (BBR-Q40-05); Mobility Scooter (BBR-Q40-06)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| September 30, 2025 | K251799 | Mobility Scooter (BBR-Q40-01); Mobility Scooter (BBR-Q40-02); Mobility Scooter (BBR-Q40-03); Mobility Scooter (BBR-Q40-04); Mobility Scooter (BBR-Q40-05); Mobility Scooter (BBR-Q40-06) | INI | Substantially Equivalent | Jiangsu Bangbang Intelligent Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 30, 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.