Allergan, Inc. - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
FDA 510(k) cleared devices by Allergan, Inc. Ophthalmic ✕
29 devices
Cleared
Aug 08, 2019
REFRESH RELIEVA For CONTACTS
Ophthalmic
146d
Cleared
Nov 21, 2016
XEN Glaucoma Treatment System
Ophthalmic
179d
Cleared
Jul 09, 2009
REFRESH OPTIVE LENS COMFORT REWETTING DROPS
Ophthalmic
199d
Cleared
Feb 20, 2002
COMPLETE BRAND MULTI-PURPOSE SOLUTION
Ophthalmic
61d
Cleared
Feb 11, 2002
COMPLETE BRAND MULTI-PURPOSE SOLUTION
Ophthalmic
115d
Cleared
Feb 21, 2001
COMPLETE BRAND MULTI-PURPOSE SOLUTION
Ophthalmic
127d
Cleared
Feb 13, 2001
MOJAVE CATARACT EXTRACTION SYSTEM
Ophthalmic
81d
Cleared
Nov 21, 2000
COMPLETE BRAND LUBRICATING AND REWETTING DROPS
Ophthalmic
48d
Cleared
Jun 02, 2000
COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION
Ophthalmic
135d
Cleared
Oct 07, 1999
REFRESH CONTACTS LUBRICATING AND REWETTING DROPS
Ophthalmic
113d
Cleared
Dec 18, 1998
ULTRACARE NEUTRALIZING TABLETS
Ophthalmic
10d
Cleared
Nov 25, 1998
COMPLETE BRAND LUBRICATING AND REWETTING DROPS
Ophthalmic
77d