Data / Medical devices / China / Jiangsu Pinkang Medical Technology Co Ltd
Jiangsu Pinkang Medical Technology Co Ltd: FDA-registered device maker in Danyang Jiangsu, China, 1 510(k) clearance
Jiangsu Pinkang Medical Technology Co Ltd is registered with the FDA (registration 3015220328) in Danyang Jiangsu, China. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 29, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015220328
- Address
- No. 138, zhenxing Road, Danyang Jiangsu, China, 212300
- Owner or operator
- JIANGSU PINKANG MEDICAL TECHNOLOGY CO LTD (10059731)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- February 17, 2019
- Registered through
- 2026
- Brand names listed
- 146-D574-BR 3 Position Recliner Blue Ridge,, 146-D574-J 3 Position Recliner Jade,, 146-D574-R 3Position Recliner Rosewood,, 146-D574EW-BR 3 Position Recliner Blue Ridge ExtraWide,, 146-D574EW-J 3 Position Recliner Jade ExtraWide,, 146-D574EW-R 3 Position Recliner Rosewood ExtraWide,, Bariatric Commode LVA1059, Bath Chair, Four-Wheel Bath Chair, No Backrest Bath Chair, Shower Chair, Bath Bench Chair ,Raised Toilet Seat ,Toilet Safety Rail and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Manufacturer | accessdata.fda.gov |
| Attachment, Commode, Wheelchair | INB | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Geriatric | FRJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Crutch | IPR | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Table, Mechanical | INW | 1 | Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Contract manufacturer, 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 29, 2019 | K190534 | Manual Wheelchair SIVFH2A102 | IOR | Substantially Equivalent | Jiangsu Horizon Medical Science & Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Adaptor, Hygiene
- All makers of Attachment, Commode, Wheelchair
- All makers of Table, Mechanical
- All makers of Wheelchair, Mechanical
- All makers of Walker, Mechanical
- All makers of Crutch
Updated May 29, 2019. 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.