Data / Medical devices / Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) / Taiwan
FDA-registered makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) in Taiwan: 8 establishments
8 establishments in Taiwan are registered with the FDA to make Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) (product code DWL). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
- Product code
- DWL
- Country
- Taiwan
Makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| I-Ming Sanitary Materials Co., Ltd. | Changhua, Taiwan | Manufacturer | 1 | August 3, 2010 | 0 | 0 | 0 | api.fda.gov |
| Power Well Healthcare Technology Co., Ltd. | Changhua County, Taiwan | Exporter to the US, Manufacturer | 1 | August 3, 2010 | 0 | 0 | 0 | api.fda.gov |
| Comfort Plus Corporation | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Da Yu Enterprise Co., Ltd. | Tianzhong Township Changhua, Taiwan | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pintoli Enterprises Co., Ltd. | Changhua County, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rich Joy Co., Ltd. | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sun Polar International Co., Ltd. | Changhua County, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yasco Enterprise Corp. | Chiayi County Chiayi(County), Taiwan | Exporter to the US, 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.