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Data / Medical devices / United States / United Contact Lens Inc

United Contact Lens Inc: FDA-registered device maker in Arlington, WA, United States, 2 510(k) clearances

United Contact Lens Inc is registered with the FDA (registration 2918644) in Arlington, WA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 1, 2005. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2918644
Address
19111 61st Ave Ne Unit 5, Arlington, WA, United States, 98223
Owner or operator
UNITED CONTACT LENS INC (10095157)
Roles
Manufacturer
First device listed
January 29, 2026
Registered through
2026
Brand names listed
55 Multifocal, 55 SV, 55 Toric, UCL Multifocal

Devices it lists

DeviceProduct codeClassRoleSource
Lenses, Soft Contact, Daily WearLPL2Manufactureraccessdata.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
July 1, 2005K05118455 SV, MULTIFOCAL AND TORIC (OCUFILCON C) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEARLPLSubstantially EquivalentUnited Contact Lens, Inc.accessdata.fda.gov
June 6, 1994K941607UCL MULTIFOCAL SOFT CONTACT LENSLPLSubstantially EquivalentUnited Contact Lens, Inc.accessdata.fda.gov

Compare with other makers

Updated July 1, 2005. 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.