Data / Medical devices / China / Danyang Chanxin Glasses Cases Factory
Danyang Chanxin Glasses Cases Factory: FDA-registered device maker in Danyang Jiangsu, China, 1 510(k) clearance
Danyang Chanxin Glasses Cases Factory is registered with the FDA (registration 3013433228) in Danyang Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 7, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013433228
- Address
- Huadian Innovation Park, Dangui Road, Development Zone, Danyang Jiangsu, China, 212300
- Owner or operator
- DANYANG CHANXIN GLASSES CASES FACTORY (10053069)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- October 28, 2016
- Registered through
- 2026
- Brand names listed
- M-BTB
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | 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 |
|---|---|---|---|---|---|---|
| June 7, 2016 | K160005 | Contact Lens Case (multiple brand name) | LRX | Substantially Equivalent | Danyang Chanxin Glasses Cases Factory | accessdata.fda.gov |
Compare with other makers
Updated June 7, 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.