Data / Medical devices / China / Xiantao S&J Protective Products Co., Ltd
Xiantao S&J Protective Products Co., Ltd: FDA-registered device maker in Xiantao Hubei, China, 1 510(k) clearance
Xiantao S&J Protective Products Co., Ltd is registered with the FDA (registration 3011434305) in Xiantao Hubei, China. It lists 41 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 19, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011434305
- Address
- 18 Zhijin Road, Pengchang, Xiantao Hubei, China, 433000
- Owner or operator
- Xiantao S&J Protective Products Co., Ltd (10058294)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 26, 2018
- Registered through
- 2026
- Brand names listed
- Absorbent Paper Points, Adhesive bandage, Air/Water Syringe Tips, Curved Utility Syringes, Alcohol Pad, Hand Sanitizer, Medical Alcohol, Medical Devices Sanitizer Spray, Antiseptic Towelette, Barrier Sleeves, Bedsheet, Bed Sheet Roll, Bedcover, Pillowcase, Body Bag, Underpad, Crepe Paper Roll, Drape Sheet, Table Cover, Cotton Roll, Cotton Tip Applicators 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 |
|---|---|---|---|---|---|---|
| August 19, 2021 | K211462 | Disposable Ear-loop Medical Face Mask, Disposable Tie-On Medical Face Mask | FXX | Substantially Equivalent | Xiantao S&J Protective Products Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Applicator, Absorbent Tipped, Non-Sterile
- All makers of Mask, Scavenging
- All makers of Apron, Protective
- All makers of Disinfectant, Medical Devices
- All makers of Basin, Emesis
- All makers of Gauze/Sponge, Internal, X-Ray Detectable
Updated August 19, 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.