Data / Medical devices / Taiwan / Action Eyewear Corp.
Action Eyewear Corp.: FDA-registered device maker in Tainan, Taiwan, 1 510(k) clearance
Action Eyewear Corp. is registered with the FDA (registration 3006112861) in Tainan, Taiwan. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006112861
- Address
- No.193, Alley 71, Lane 942, Tawan Road Yungkang District, Tainan, Taiwan, 71070
- Owner or operator
- ACTION EYEWEAR CORP. (9005980)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- August 4, 1992
- Registered through
- 2026
- Brand names listed
- 9&CO, ANDREA JOVINE, ANN TAYLOR FACTORY, APPLES BOTTOMS, Allen B Schwartz, Andrew Marc, BCBGMAXAZRIA, BETSEY JOHNSON and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | Exporter to the US | accessdata.fda.gov |
| Frame, Spectacle | HQZ | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| June 6, 2000 | K991206 | BONASSE CONTACT LENS CASE | LRX | Substantially Equivalent | Bonasse Ent. Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Frame, Spectacle
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Case, Contact Lens
- All makers of Spectacle, Magnifying
- All makers of Sunglasses (Non-Prescription Including Photosensitive)
Updated June 6, 2000. 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.