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Data / Medical devices / Taiwan / Yung Sheng Optical Co., Ltd.

Yung Sheng Optical Co., Ltd.: FDA-registered device maker in Taichung City, Taiwan, 10 510(k) clearances

Yung Sheng Optical Co., Ltd. is registered with the FDA (registration 3004021238) in Taichung City, Taiwan. It lists 2 device types. The FDA files 10 510(k) clearances under its listings, the newest dated September 25, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004021238
Address
No. 8, Keya 2nd Road Daya District, Taichung City, Taiwan, 42881
Owner or operator
Yung Sheng Optical Co., Ltd. (10047700)
Roles
Foreign private label distributor, Manufacturer
First device listed
October 21, 2014
Registered through
2026
Brand names listed
Air Light 38 UV Aspheric (polymacon) Soft (hydrophilic) Contact Lens for Daily Wear, Eye Secret, Eye Secret 38 UV Aspheric (polymacon) Soft (hydrophilic) Contact Lens for Daily Wear, Eye Secret 38 UV Aspheric Color (polymacon) 1-Day Soft (hydrophilic) Contact Lens, Eye Secret 38 UV Aspheric Color (polymacon) Soft (hydrophilic) Contact Lens for Daily Wear, Eye Secret 55 UV Aspheric (methafilcon A) Soft (hydrophilic) Contact Lens, Pure Plus UV Aspheric (Otufilcon A) 1-Day Silicone Soft (hydrophilic) Contact Lens (Daily Disposable), Pure Plus UV Aspheric (Otufilcon A) Silicone Soft (hydrophilic) Contact Lens for Daily Wear (Daily Wear) and more

Devices it lists

DeviceProduct codeClassRoleSource
Lens, Contact, (Disposable)MVN2Foreign private label distributor, Manufactureraccessdata.fda.gov
Lenses, Soft Contact, Daily WearLPL2Foreign private label distributor, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 25, 2025K244009Pure Plus UV Aspheric (Otufilcon A) Silicone Soft (hydrophilic) Contact Lens for Daily Wear (Daily Wear); Pure Plus UV Aspheric (Otufilcon A) 1-Day Silicone Soft (hydrophilic) Contact Lens (Daily Disposable)LPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
December 16, 2024K232839Eye Secret 38 UV Aspheric (polymacon) and Air Light 38 UV Aspheric (polymacon) Soft (hydrophilic) Contact Lens for Daily WearLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
December 20, 2023K223585Pure Plus UV Aspheric (Otufilcon A) Silicone Soft (hydrophilic) Contact Lens for Daily WearLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
September 2, 2022K213983Eye Secret 59 UV Aspheric (Omafilcon A) Soft (Hydrophilic) Contact Lens for Daily WearLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
August 10, 2015K151586Eye Secret 55 UV Aspheric (Methafilcon A) Soft (hydrophilic) Contact LensLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
June 15, 2015K150630Eye Secret 38 UV Aspheric (polymacon) Soft (hydrophilic) Contact Lens for Daily Wear, Eye Secret 55 UV Aspheric ( methafilcon A) Soft (hydrophilic) Contact lens for Daily WearMVNSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
January 16, 2015K143190Eye Secret 38 UV Aspheric (polymacon) 1-Day Soft (hydrophilic) Contact LensMVNSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
December 16, 2014K143052Eye Secret 38 UV Aspheric Color(polymacon) Soft(hydrophilic) Contact Lens for Daily;Eye Secret 38 UV Aspheric Color(polymacon) 1-Day Soft(hydrophilic) Contact LensLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
March 21, 2014K133735EYE SECRET 55 UV ASPHERIC (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENSLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov
December 23, 2013K132854EYE SECRET 38 UV ASPHERIC (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEARLPLSubstantially EquivalentYung Sheng Optical Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 25, 2025. 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.