Data / Medical devices / Lenses, Soft Contact, Daily Wear / Taiwan
FDA-registered makers of Lenses, Soft Contact, Daily Wear in Taiwan: 8 establishments
8 establishments in Taiwan are registered with the FDA to make Lenses, Soft Contact, Daily Wear (product code LPL). 8 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
- Taiwan
Makers of Lenses, Soft Contact, Daily Wear in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Pegavision Corporation | Taoyuan, Taiwan | Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer | 15 | May 21, 2026 | 0 | 0 | 0 | api.fda.gov |
| Pegavision Corporation-Daxi | Taoyuan City, Taiwan | Complaint file establishment, Exporter to the US, Manufacturer | 15 | May 21, 2026 | 0 | 0 | 0 | api.fda.gov |
| ST. Shine Optical Co., Ltd. | Hsi Chih Dist, New Taipei City, Taiwan | Manufacturer | 13 | March 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Yung Sheng Optical Co., Ltd. | Taichung City, Taiwan | Foreign private label distributor, Manufacturer | 8 | September 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Innova Vision Inc. | Hsinchu City, Hsinchu(City), Taiwan | Manufacturer | 5 | April 17, 2024 | 0 | 0 | 0 | api.fda.gov |
| Vizionfocus Inc. | Zhunan Township Miaoli, Taiwan | Manufacturer | 5 | September 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Unicon Optical Co., Ltd. | Hsinchu County Hsinchu(County), Taiwan | Contract manufacturer, Exporter to the US, Manufacturer | 4 | January 18, 2022 | 0 | 0 | 0 | api.fda.gov |
| Seinoh Optical Co., Ltd | New Taipei City, Taiwan | Manufacturer | 1 | July 18, 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.