Data / Medical devices / China / Yangjiang Junchang Trading Co., Ltd
Yangjiang Junchang Trading Co., Ltd: FDA-registered device maker in YANGJIANG Guangdong, China, 1 510(k) clearance
Yangjiang Junchang Trading Co., Ltd is registered with the FDA (registration 3009097913) in YANGJIANG Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 17, 1989. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009097913
- Address
- No.39 Baiyun Road, YANGJIANG Guangdong, China, 529500
- Owner or operator
- YANGJIANG JUNCHANG TRADING CO., LTD (10089175)
- Roles
- Exporter to the US
- First device listed
- November 10, 2023
- Registered through
- 2026
- Brand names listed
- Grafco, Grafco Eye Shield
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Block, Bite | JXL | 2 | Exporter to the US | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Exporter to the US | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | 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 |
|---|---|---|---|---|---|---|
| February 17, 1989 | K890567 | BITE BLOCK #59430 | JXL | Substantially Equivalent | Medi-Source, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Container, Liquid Medication, Graduated
- All makers of Block, Bite
Updated February 17, 1989. 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.