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Data / Medical devices / United States / Valley Contax, Inc

Valley Contax, Inc: FDA-registered device maker in Eugene, OR, United States, 1 510(k) clearance

Valley Contax, Inc is registered with the FDA (registration 3022320387) in Eugene, OR, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 7, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3022320387
Address
4748 Franklin Boulevard, Eugene, OR, United States, 97403
Owner or operator
Valley Contax (10053951)
Roles
Contract manufacturer, Manufacturer
First device listed
January 25, 2017
Registered through
2026
Brand names listed
11.2 Specialty, APK, ATS, C.E.L.L, C.E.L.L., CAD, CAD Fixed, Comfort XL and more

Devices it lists

DeviceProduct codeClassRoleSource
Lens, Contact (Other Material) - DailyHQD2Contract manufacturer, 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 7, 2022K213880Custom Stable Rigid Gas Permeable Scleral Contact LensHQDSubstantially EquivalentValley Contax, Inc.accessdata.fda.gov

Compare with other makers

Updated January 7, 2022. 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.