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Data / Medical devices / Thailand / HOYA LAMPHUN LTD., HOYA Eye Care Thailand

HOYA LAMPHUN LTD., HOYA Eye Care Thailand: FDA-registered device maker in Amphur Muang Lamphun, Thailand, 1 510(k) clearance

HOYA LAMPHUN LTD., HOYA Eye Care Thailand is registered with the FDA (registration 3045742980) in Amphur Muang Lamphun, Thailand. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 3, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045742980
Address
Northern Region Industrial Estate, 75/2 Moo 4, Tambol Banklang, Amphur Muang Lamphun, Thailand, 51000
Owner or operator
HOYA Lamphun Ltd. (10095878)
Roles
Complaint file establishment, Exporter to the US, Manufacturer
First device listed
May 14, 2026
Registered through
2026
Brand names listed
ILLUMINA 1 DAY Multifocal Soft silicone hydrogel contact lens, ILLUMINA 1 DAY Soft silicone hydrogel contact lens, ILLUMINA 1 DAY Toric Soft silicone hydrogel contact lens

Devices it lists

DeviceProduct codeClassRoleSource
Lens, Contact, (Disposable)MVN2Complaint file establishment, Exporter to the US, Manufactureraccessdata.fda.gov
Lenses, Soft Contact, Daily WearLPL2Complaint file establishment, Exporter to the US, 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
January 3, 2024K223397HOYA Illumina (sorafilcon A) Daily Disposable Soft Contact Lens, HOYA Illumina (sorafilcon A) Toric Daily Disposable Soft Contact Lens, HOYA Illumina (sorafilcon A) Multifocal Daily Disposable Soft Contact LensLPLSubstantially EquivalentHoya Lamphun , Ltd.accessdata.fda.gov

Compare with other makers

Updated January 3, 2024. 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.