Data / Medical devices / China / Aosom E-Commerce Inc
Aosom E-Commerce Inc: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance
Aosom E-Commerce Inc is registered with the FDA (registration 3011962812) in Ningbo Zhejiang, China. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 9, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011962812
- Address
- 6-9 F, Middle Tower of MH Mansion,288 Xi-Lu Road, Zhuangshi Street,Zhenhai District, Ningbo Zhejiang, China, 315201
- Owner or operator
- Aosom E-Commerce Inc (10057733)
- Roles
- Exporter to the US
- First device listed
- May 18, 2018
- Registered through
- 2026
- Brand names listed
- Electric wheelchair, Knee walker,Rollator,walker, Massage Recliner, Massage Sofa, Powered wheelchair, Raised toilet seat,Commode chairs, Shower chair,Safety rail
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Exporter to the US | accessdata.fda.gov |
| Attachment, Commode, Wheelchair | INB | 1 | Exporter to the US | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Exporter to the US | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Exporter to the US | 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 9, 2017 | K170787 | Powered Wheelchair DYW30A(D09) | ITI | Substantially Equivalent | Nanjing Jin Bai HE Medical Apparatus Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Walker, Mechanical
- All makers of Attachment, Commode, Wheelchair
- All makers of Adaptor, Hygiene
- All makers of Wheelchair, Powered
- All makers of Massager, Therapeutic, Electric
Updated August 9, 2017. 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.