Data / Medical devices / China / Suzhou Zhenwu Medical Co., Ltd.
Suzhou Zhenwu Medical Co., Ltd.: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Suzhou Zhenwu Medical Co., Ltd. is registered with the FDA (registration 3007740684) in Suzhou Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 10, 2023. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007740684
- Address
- No.248, Chijiawan Road, Beishe Town Fenhu Development Area, Wujiang District, Suzhou Jiangsu, China, 215214
- Owner or operator
- Suzhou Zhenwu Medical Co., Ltd. (10029917)
- Roles
- Manufacturer
- First device listed
- July 15, 2009
- Registered through
- 2027
- Brand names listed
- Auto Lancets:Button Activated Safety Lancet(BA) 18G~36G, Auto Lancets:Pressure Activated Safety Lancet(PA) 18G~36G, Blood Lancet, Flat blood lancets 28G~36G, Lancet Device with Ejector, Lancets with Pull Tops, Lancing Devices S L, Lancing Devices With Blood Lancets and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | 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 |
|---|---|---|---|---|---|---|
| February 10, 2023 | K223208 | Safety Lancet | FMK | Substantially Equivalent | Suzhou Zhenwu Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 10, 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.