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Allergan Sales, LLC

United States·US-MF-000001517

Last updated September 17, 2026

Information

Country
United States
Address
2525, Dupont Drive, Irvine, California, United States
Website
abbvie.com
LinkedIn
—
Facebook
—
Phone
+1 (800) 678-1605
PRRC Contact
Angela Iyer
EUDAMED SRN
US-MF-000001517
FDA FEI Number
2011068
DUNS Number
—

Catalogue (94)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Optive Fusion 94607UC
EUDAMED
Class IIbActive
Optive Advance 96465GB
EUDAMED
Class IIbActive
Keller Funnel 2 HA-001
EUDAMEDFDA UDI
Class IIaActive
Optive Plus Ud 94542FC
EUDAMED
Class IIbActive
Cellufresh 91951EW
EUDAMED
Class IIbActive
Optive Plus 94307CZ
EUDAMED
Class IIbActive
Optive Ud 93416EH
EUDAMED
Class IIbActive
Optava Advance 96465EK
EUDAMED
Class IIbActive
Optive Fusion 94607EL
EUDAMED
Class IIbActive
Optive Fusion 94607FH
EUDAMED
Class IIbActive
Optive Fusion 94606CM
EUDAMED
Class IIbActive
Cellumed 92056EW
EUDAMED
Class IIbActive
Optive Plus 94307EH
EUDAMED
Class IIbActive
Optive Fusion 94606YB
EUDAMED
Class IIbActive
Liquifilm Tears 95389GB
EUDAMED
Class IIbActive
Refresh Contacts 91962UC
EUDAMED
Class IIbActive
Optive Advance 96465CM
EUDAMED
Class IIbActive
Optive Advance 96615TC
EUDAMED
Class IIbActive
Skin Marking Grid 95729EU
EUDAMED
Class IActive
Optive Plus 94306GB
EUDAMED
Class IIbActive
Optive Fusion Ud 94515IT
EUDAMED
Class IIbActive
Optive Plus 94307EW
EUDAMED
Class IIbActive
Lacrilube 22395FR
EUDAMED
Class IIbActive
Xen 63 Glaucoma Treatment System 5501-001
EUDAMED
Class IIIActive
Optava Ud 93416EK
EUDAMED
Class IIbActive
Optive Fusion Ud 94515EW
EUDAMED
Class IIbActive
Optive Fusion Ud 97034AQ
EUDAMED
Class IIbActive
Optive Ud 93416EW
EUDAMED
Class IIbActive
Optive 93304FP
EUDAMED
Class IIbActive
Liquifilm® O.k. N 95395EW
EUDAMED
Class IIbActive
Optive Gel Drops 95459FH
EUDAMED
Class IIbActive
Keller Funnel 2 HA-005
EUDAMEDFDA UDI
Class IIaActive
Optava Fusion Ud 94515EK
EUDAMED
Class IIbActive
Optive 93304EW
EUDAMED
Class IIbActive
Optava Fusion 94606EM
EUDAMED
Class IIbActive
Optive Fusion Ud 95537TC
EUDAMED
Class IIbActive
Lacrimal® O.k. N 95392EW
EUDAMED
Class IIbActive
Refresh Ud 95388EJ
EUDAMED
Class IIbActive
Refresh Tears 91962HB
EUDAMED
Class IIbActive
Liquifilm 93625EW
EUDAMED
Class IIbActive
Optive 93304XZ
EUDAMED
Class IIbActive
Optive Fusion 94606SW
EUDAMED
Class IIbActive
Optava Gel Drops 95382EM
EUDAMED
Class IIbActive
Liquifilm Tears 95388GB
EUDAMED
Class IIbActive

Related Companies

Importers

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Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Mar 14, 2024Z-1694-2024—open, classified

Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.