Data / Medical devices / China / Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.: FDA-registered device maker in Chengdu Sichuan, China, 1 510(k) clearance
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. is registered with the FDA (registration 3004099493) in Chengdu Sichuan, China. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004099493
- Address
- NO. 51, 4th Group Wanjie Village, Baodun Town, 611438 Xinjin District NO. 3561, Xixin Avenue, Puxing Street, 611435 Xinjin District, Chengdu Sichuan, China, 611438
- Owner or operator
- Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., L (10056352)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 30, 2017
- Registered through
- 2026
- Brand names listed
- Dental Syrnge, Enteral Syringe, Insulin Syringe, Irrigating syringe, NuGen Syringe, Oral Syringe, PC Syringe, PISTON SYRINGE and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Liquid Medication, Graduated | KYW | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Enteral Syringes With Enteral Specific Connectors | PNR | 2 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Contract manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Dental) | EIB | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| System, Urine Drainage, Closed, For Non-Indwelling Catheter, Non-Sterile | NNZ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Contract 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 25, 2016 | K152808 | U&U Insulin Syringe with/without Safety Retractable Device | MEG | Substantially Equivalent | U&U Medical Technology Co, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Antistick
- All makers of Syringe, Piston
- All makers of System, Urine Drainage, Closed, For Non-Indwelling Catheter, Non-Sterile
- All makers of Enteral Syringes With Enteral Specific Connectors
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Tubing, Noninvasive
Updated March 25, 2016. 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.