Data / Medical devices / Attachment, Narrowing, Wheelchair
Attachment, Narrowing, Wheelchair (IMQ): 8 FDA-registered makers in 4 countries
8 establishments in 4 countries are registered with the FDA to make Attachment, Narrowing, Wheelchair (product code IMQ, Class 1, 21 CFR 890.3920). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IMQ
- Device class
- 1
- Regulation
- 890.3920
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| China | 5 |
| Canada | 1 |
| New Zealand | 1 |
| Sweden | 1 |
Makers of Attachment, Narrowing, Wheelchair
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Broda LP | Kitchener Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hangzhou Rollmed Co.,ltd. | Hangzhou Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Sintang Health&technology Co.,ltd | Yancheng Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Metalform Ltd | Dannevirke Hawke's Bay, New Zealand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Permobil (kunshan) Co., Ltd | Kunshan Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Permobil AB | Sundsvall Vasternorrland, Sweden | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Permobil Trading (kunshan) Co., Ltd | Kunshan Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhongshan Saxin Electric Heating Technology Co., Ltd. | Zhongshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.