Data / Medical devices / China / Xiantao Daoqi Plastic Co., Ltd.
Xiantao Daoqi Plastic Co., Ltd.: FDA-registered device maker in Xiantao Hubei, China, 1 510(k) clearance
Xiantao Daoqi Plastic Co., Ltd. is registered with the FDA (registration 3011140825) in Xiantao Hubei, China. It lists 16 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 18, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011140825
- Address
- NO. 83 Wagou New District Pengchang Town, Xiantao Hubei, China, 433018
- Owner or operator
- Xiantao Daoqi Plastic Co., Ltd. (10048250)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- December 20, 2014
- Registered through
- 2026
- Brand names listed
- Coverall, Disposable Coverall, Diposable Surgical Instrument, Disposable Dress, Dress, Surgical, Drape, surgical, Face Mask, Nonwoven Face Mask, Disposable Face Mask, Nonwoven Cap, Bouffant Cap, Disposable Cap, Plastic Cap, Doctor Cap, Surgical cap, Nonwoven Fabric, Melt-blown Fabric,Disposable Diaper, Fiber, Medical, Absorbent, Shoe Cover,Boot Cover, Plastic Shoe Cover, Nonwoven Shoe Cover, Plastic Boot Cover, Nonwoven Boot Cover and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| October 18, 2024 | K240916 | Surgical Face Mask (Tie on/ Ear loops) | FXX | Substantially Equivalent | Xiantao Daoqi Plastic Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mask, Scavenging
- All makers of Cover, Cast
- All makers of Accessory, Surgical Apparel
- All makers of Board, Arm (With Cover), Non-Sterile
- All makers of Drape, Surgical, Antimicrobial
- All makers of Mask, Surgical
Updated October 18, 2024. 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.