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Data / Medical devices / Ireland / Allergan Pharmaceuticals Ireland

Allergan Pharmaceuticals Ireland: FDA-registered device maker in WESTPORT Mayo, Ireland, 1 510(k) clearance

Allergan Pharmaceuticals Ireland is registered with the FDA (registration 8020862) in WESTPORT Mayo, Ireland. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 8, 2019. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number
8020862
FEI number
3002806285
Address
Castlebar RD., WESTPORT Mayo, Ireland, --
Owner or operator
AbbVie, Inc. (2011068)
Roles
Manufacturer
First device listed
August 23, 2019
Registered through
2027
Brand names listed
REFRESH® RELIEVA™ For CONTACTS

Devices it lists

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
August 8, 2019K190674REFRESH RELIEVA For CONTACTSLPNSubstantially EquivalentAllergan, Inc.accessdata.fda.gov

Compare with other makers

Updated August 8, 2019. 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.