Data / Medical devices / China / Well Care (wuhan) Medical Technology Co., Ltd.
Well Care (wuhan) Medical Technology Co., Ltd.: FDA-registered device maker in Wuhan Hubei, China, 1 510(k) clearance
Well Care (wuhan) Medical Technology Co., Ltd. is registered with the FDA (registration 3022555975) in Wuhan Hubei, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3022555975
- Address
- No. 11# The No.1 road Fozuling of East Lake High-Tech Development Zone, Wuhan Hubei, China, 430205
- Owner or operator
- Well care (Wuhan) medical technology Co., Ltd. (10084681)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- March 21, 2022
- Registered through
- 2026
- Brand names listed
- Automatic Tightening Band Ligation for Hemorrhoids, Female urinary collection system, Quantitative Tighten Elastic Thread Ligator for Hemorrhoids, Speculum, Rectal, WellCare Anoscope
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Anoscope And Accessories | FER | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Ligator, Hemorrhoidal | FHN | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Speculum, Rectal | FFQ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Urinary Drainage Collection Kit, For Indwelling Catheter | FCN | 2 | 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 |
|---|---|---|---|---|---|---|
| December 22, 2023 | K230439 | WellCare Anoscope | FER | Substantially Equivalent | Well Care (Wuhan) Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Ligator, Hemorrhoidal
- All makers of Urinary Drainage Collection Kit, For Indwelling Catheter
- All makers of Anoscope And Accessories
- All makers of Speculum, Rectal
Updated December 22, 2023. 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.