Data / Medical devices / China / Csic (HK) Company
Csic (HK) Company: FDA-registered device maker in Yiwu Zhejiang, China, 1 510(k) clearance
Csic (HK) Company is registered with the FDA (registration 3012409043) in Yiwu Zhejiang, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 29, 1996. Registered through 2027. FDA data exported November 2, 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
- 3012409043
- Address
- Room 203, Unit 2, Building 6, Futian 2nd Area, Yiwu Zhejiang, China, 322000
- Owner or operator
- csic (hk) company (10055398)
- Roles
- Manufacturer
- First device listed
- July 19, 2017
- Registered through
- 2027
- Brand names listed
- CSIC SUNGLASSES
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Frame, Spectacle | HQZ | 1 | Manufacturer | accessdata.fda.gov |
| Lens, Spectacle, Non-Custom (Prescription) | HQG | 1 | Manufacturer | accessdata.fda.gov |
| Spectacle, Magnifying | HOI | 1 | Manufacturer | accessdata.fda.gov |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | 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 |
|---|---|---|---|---|---|---|
| January 29, 1996 | K955441 | ZONG RONG SUNGLASSES | HQY | Substantially Equivalent | Zong Rong Glasses Ltd. Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Spectacle, Magnifying
- All makers of Frame, Spectacle
- All makers of Sunglasses (Non-Prescription Including Photosensitive)
- All makers of Lens, Spectacle, Non-Custom (Prescription)
Updated January 29, 1996. 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.