Data / Medical devices / China / Ucomfor Scientific Co.,ltd
Ucomfor Scientific Co.,ltd: FDA-registered device maker in Zhangjiagang Jiangsu, China, 1 510(k) clearance
Ucomfor Scientific Co.,ltd is registered with the FDA (registration 3016884033) in Zhangjiagang Jiangsu, China. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 11, 2005. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3016884033
- Address
- Lekun Road, Leyu Town, Zhangjiagang Jiangsu, China, 215621
- Owner or operator
- Ucomfor Scientific Co.,Ltd (10067128)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- March 29, 2021
- Registered through
- 2026
- Brand names listed
- Connector, Drainage bags, Enteral Extension Sets, Feeding tubes, Nasoenteric Feeding Tubes, SUCTION YANKAUER, Yankauer, non-vented bulb/regular tip, Sterile,Yankauer, vented bulb/regular tip, Suct instr yank blb w/o vent, Yankauer, vented regular tip, Sterile, Latex Free, Suct instr yank reg w vent, TUBE, ASPIRATING, FLEXIBLE, CONNECTING, Suction conneting tube, Suction Tubing, Thumb control piston irrigation syringe 60cc ST, Bulb irrigation syringe 60cc ST, Flat top piston irrigation syringe 60c and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter And Tip, Suction | JOL | 2 | Exporter to the US | accessdata.fda.gov |
| Collector, Urine, (And Accessories) For Indwelling Catheter | KNX | 2 | Exporter to the US | accessdata.fda.gov |
| Connector, Catheter | GCD | 1 | Manufacturer | accessdata.fda.gov |
| Device, Paste-On For Incontinence, Sterile | EXI | 1 | Exporter to the US | accessdata.fda.gov |
| Device, Urine Flow Rate Measuring, Non-Electrical, Disposable | FFG | 2 | Exporter to the US | accessdata.fda.gov |
| Evacuator, Bladder, Manually Operated | FFD | 1 | Manufacturer | accessdata.fda.gov |
| Gastrointestinal Tubes With Enteral Specific Connectors | PIF | 2 | Contract manufacturer | accessdata.fda.gov |
| Speculum, Vaginal, Nonmetal | HIB | 2 | Exporter to the US | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Exporter to the US | accessdata.fda.gov |
| Tube, Aspirating, Flexible, Connecting | BYY | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| July 11, 2005 | K050887 | GONGDONG DISPOSABLE VAGINAL SPECULUM | HIB | Substantially Equivalent | Zhejiang Gongdong Medical Plastic Factory | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Paste-On For Incontinence, Sterile
- All makers of Syringe, Irrigating (Non Dental)
- All makers of Catheter And Tip, Suction
- All makers of Collector, Urine, (And Accessories) For Indwelling Catheter
- All makers of Gastrointestinal Tubes With Enteral Specific Connectors
- All makers of Speculum, Vaginal, Nonmetal
Updated July 11, 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.