Data / Medical devices / China / Safeway Industry Healthcare
Safeway Industry Healthcare: FDA-registered device maker in Xiantao Hubei, China, 1 510(k) clearance
Safeway Industry Healthcare is registered with the FDA (registration 3017450342) in Xiantao Hubei, China. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 22, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017450342
- Address
- No.106, Chang'an Road Changshangkou, Xiantao Hubei, China, -
- Owner or operator
- Safeway Industry Healthcare (10075755)
- Roles
- Manufacturer
- First device listed
- June 25, 2020
- Registered through
- 2026
- Brand names listed
- Face Mask, Non-Surgical Isolation Gown, Operating Room Shoe Cover, Surgical Cap
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cap, Surgical | FYF | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Shoe, Operating-Room | FXP | 1 | Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | 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 |
|---|---|---|---|---|---|---|
| June 22, 2021 | K210840 | Disposable Surgical Mask | FXX | Substantially Equivalent | Safeway Industry Healthcare. | accessdata.fda.gov |
Compare with other makers
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Mask, Surgical
- All makers of Cap, Surgical
- All makers of Non-Surgical Gown
- All makers of Cover, Shoe, Operating-Room
Updated June 22, 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.