Data / Medical devices / China / Hubei Deming Healthcare Products Co.,ltd.first Branch
Hubei Deming Healthcare Products Co.,ltd.first Branch: FDA-registered device maker in Xiantao City Hubei, China, 1 510(k) clearance
Hubei Deming Healthcare Products Co.,ltd.first Branch is registered with the FDA (registration 3012761602) in Xiantao City Hubei, China. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 27, 2019. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3012761602
- Address
- No.198, Pengchang Ave, Pengchang Town, Xiantao City Hubei, China, 433018
- Owner or operator
- HUBEI DEMING HEALTHCARE PRODUCTS CO.,LTD.FIRST BRANCH (10095252)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- February 11, 2026
- Registered through
- 2026
- Brand names listed
- ACCESSORY, SURGICAL APPAREL, Face mask, BEDDING, DISPASABLE, MEDICAL, CAP, SURGICAL, CHU TIAN DE MING Single use surgical mask, Face mask, Non-surgical isolation gown, Patient exam gown, Shoe Cover and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Cap, Surgical | FYF | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Cover, Shoe, Operating-Room | FXP | 1 | Exporter to the US, 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 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Exporter to the US, 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 27, 2019 | K182515 | Surgical Face Mask | FXX | Substantially Equivalent | Wuhan Dymex Healthcare Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Gown, Examination
- All makers of Non-Surgical Gown
- All makers of Cap, Surgical
- All makers of Bedding, Disposable, Medical
- 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, Scavenging
Updated May 27, 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.