Data / Medical devices / China / Shanghai Jinxiang Latex Products Co., Ltd.
Shanghai Jinxiang Latex Products Co., Ltd.: FDA-registered device maker in Shanghai, China, 4 510(k) clearances
Shanghai Jinxiang Latex Products Co., Ltd. is registered with the FDA (registration 8043142) in Shanghai, China. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 18, 2015. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 8043142
- FEI number
- 3332
- Address
- No. 36,Leizhou Road, Xinghuo Development, Fengxian District, Shanghai, China, 201419
- Owner or operator
- SHANGHAI JINXIANG LATEX PRODUCTS CO., LTD. (8043142)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- December 26, 2012
- Registered through
- 2026
- Brand names listed
- Patient Examination Gloves (Latex), Profect Examination Gloves, TULIP Natural Rubber Latex Surgeon's Glove (Powdered), Tulip Condom
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Latex Patient Examination Glove | LYY | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Surgeon'S Gloves | KGO | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| March 18, 2015 | K142992 | TULIP Natural Rubber Latex Surgeon's Glove (Powdered) | KGO | Substantially Equivalent | Shanghai Jinxiang Latex Products Co., Ltd. | accessdata.fda.gov |
| March 1, 2005 | K050360 | TULIP CONDOM | HIS | Substantially Equivalent | Shanghai Latex Factory | accessdata.fda.gov |
| October 31, 1989 | K892138 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | Substantially Equivalent | Shanghai Latex Factory | accessdata.fda.gov |
| September 11, 1989 | K893280 | PROFECT EXAMINATION GLOVES | LYY | Substantially Equivalent | Shanghai Latex Factory | accessdata.fda.gov |
Compare with other makers
Updated March 18, 2015. 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.