Data / Medical devices / Lenses, Soft Contact, Daily Wear / South Korea
FDA-registered makers of Lenses, Soft Contact, Daily Wear in South Korea: 10 establishments
10 establishments in South Korea are registered with the FDA to make Lenses, Soft Contact, Daily Wear (product code LPL). 10 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
- Lenses, Soft Contact, Daily Wear
- Product code
- LPL
- Country
- South Korea
Makers of Lenses, Soft Contact, Daily Wear in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Interojo Inc. | PYONGTAEK-CITY Gyeonggi, South Korea | Manufacturer | 7 | May 29, 2026 | 0 | 0 | 0 | api.fda.gov |
| Mi Gwang Contact Lens Co., Ltd. | Gyeongsan-si Gyeongbuk, South Korea | Manufacturer | 2 | September 27, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vision Science Co., Ltd. | Daegu, South Korea | Manufacturer | 2 | August 26, 2016 | 0 | 0 | 0 | api.fda.gov |
| DK Medivision Co., Ltd. | Seobuk-gu Cheonan-si Chungnam, South Korea | Manufacturer | 1 | August 5, 2022 | 0 | 0 | 0 | api.fda.gov |
| DreamCon Co. Ltd. | Yangsan-si Gyeongnam, South Korea | Manufacturer | 1 | June 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| E.O.S Co., Ltd. | Dong-gu Daegu, South Korea | Manufacturer | 1 | July 30, 2025 | 0 | 0 | 0 | api.fda.gov |
| Geo Medical Co., Ltd | Jeonnam-Gwangju, South Korea | Manufacturer | 1 | April 26, 2012 | 0 | 0 | 0 | api.fda.gov |
| Joowon Innovation Co., Ltd. | Cheonan-si, Seobuk-gu Chungnam, South Korea | Manufacturer | 1 | August 22, 2016 | 0 | 0 | 0 | api.fda.gov |
| Neo Vision Co., Ltd. | WONJU Gangwon, South Korea | Manufacturer | 1 | October 7, 2014 | 0 | 0 | 0 | api.fda.gov |
| Vassen Co., Ltd. | Pyeongtaek-si Gyeonggi, South Korea | Manufacturer | 1 | October 7, 2014 | 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.