Data / Medical devices / China / Nipro (shanghai) Co., Ltd.
Nipro (shanghai) Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance
Nipro (shanghai) Co., Ltd. is registered with the FDA (registration 3004138517) in Shanghai, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 10, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004138517
- Address
- 2555 Baoan Road Malu Town, Jading District, Shanghai, China, 201801
- Owner or operator
- NIPRO CORPORATION (8030375)
- Roles
- Manufacturer
- First device listed
- December 16, 2005
- Registered through
- 2026
- Brand names listed
- Nipro Hypodermic Needle
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 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 |
|---|---|---|---|---|---|---|
| November 10, 2005 | K052474 | NIPRO HYPODERMIC NEEDLE | FMI | Substantially Equivalent | Nipro Medical Corp. | accessdata.fda.gov |
Compare with other makers
Updated November 10, 2005. 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.