Data / Medical devices / China / Jerry Medical Instrument (shanghai) Co., Ltd.
Jerry Medical Instrument (shanghai) Co., Ltd.: FDA-registered device maker in Shanghai, China, 2 510(k) clearances
Jerry Medical Instrument (shanghai) Co., Ltd. is registered with the FDA (registration 3011707750) in Shanghai, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 13, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011707750
- Address
- Room 116, Block A, Building 1, No. 288 Jiachang Road, Malu Town, Jiading District, Shanghai, China, 201800, Shanghai, China, 201801
- Owner or operator
- Jerry Medical Instrument (Shanghai) Co., Ltd. (10082941)
- Roles
- Manufacturer
- First device listed
- October 14, 2021
- Registered through
- 2026
- Brand names listed
- Electric Wheelchair [Models: Jrwd6010/Jrwd6012], 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 |
|---|---|---|---|---|---|---|
| July 13, 2021 | K192739 | Electric Wheelchair [Models: JRWD6010/JRWD6012] | ITI | Substantially Equivalent | Jerry Medical Instrument (Shanghai) Co., Ltd. | accessdata.fda.gov |
| April 1, 2020 | K192658 | Manual Wheelchair | IOR | Substantially Equivalent | Jerry Medical Instrument (Shanghai) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 13, 2021. 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.