Data / Medical devices / Frame, Spectacle / South Korea
FDA-registered makers of Frame, Spectacle in South Korea: 31 establishments
31 establishments in South Korea are registered with the FDA to make Frame, Spectacle (product code HQZ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Frame, Spectacle
- Product code
- HQZ
- Country
- South Korea
Makers of Frame, Spectacle in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Blue Elephant.co.,ltd. | Seongdong-gu Seoul, South Korea | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coptiq Co.,ltd. | Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DR International | Buk District Jeonnam, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DUNUN Co., Ltd. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Elite Eyewear Co. | Daegu, South Korea | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eye Topic Optical Co.,ltd. | Seo-gu Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| FIVE STAR EYEWEAR CO., Ltd. | BUKGU Daegu, South Korea | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frame-Tec Co., Ltd. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frame Corporation | Suseong-gu Daegu, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| H2C Design Inc. | Buk-Gu Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hwa Sung Optical Co. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IICOMBINED Co., Ltd. | Seongdong-gu Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| James Optical Co., Ltd | BUGGU Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JCS International Co.,ltd | Gumi Gyeongbuk, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jeongs Optical | Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jinsung Optical Co. | Daegu, South Korea | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Korea Ogk Co., Ltd. | Chilgok-gun Gyeongbuk, South Korea | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Korea Optical Industry Coop. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kunhwa Optical Corporation | Daegu City, South Korea | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maxi Eye | Daegu Gyeongbuk, South Korea | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onnury Optical Co. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SA Vision Eyewear | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Samil Enterprise Company | Gyeongbuk, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SAMSUNG ELECTRONICS CO., LTD. Mobile eXperience Business AR | Suwon Gyeonggi, South Korea | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Samwon Innotech Co., Ltd. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Seeone Eyewear | Seoul, South Korea | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Seesun Co., Ltd. | Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stardream Co.,ltd. | Gangdong-gu Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| StoH | Buk-gu Daegu, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tomato Glasses | Seo-gu Busan, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Verdi Eyewear | Daegu, South Korea | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.