Data / Medical devices / Taiwan / Millson Eyewear Co Ltd
Millson Eyewear Co Ltd: FDA-registered device maker in Tainan City, Taiwan, 1 510(k) clearance
Millson Eyewear Co Ltd is registered with the FDA (registration 3007620166) in Tainan City, Taiwan. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 13, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007620166
- Address
- No.163,Sec.2,Heshun Rd.,Kuei-Jen Dist., Tainan City, Taiwan, 71145
- Owner or operator
- Millson Eyewear Co Ltd (10029557)
- Roles
- Manufacturer
- First device listed
- May 30, 2009
- Registered through
- 2026
- Brand names listed
- Reading Glasses, Safety Goggles, Spectacle Frame, Sunglasses
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Frame, Spectacle | HQZ | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 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 |
|---|---|---|---|---|---|---|
| December 13, 1994 | K945351 | SHIELD, EYE, OPHTHALMIC | HOY | Substantially Equivalent | Taiwan Eva Industrial Co., 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 Spectacle, Magnifying
- All makers of Frame, Spectacle
- All makers of Sunglasses (Non-Prescription Including Photosensitive)
Updated December 13, 1994. 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.