Allergan Medical Optics is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allergan Medical Optics - FDA 510(k) Cleared Devices
Recent clearances: AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM, AMO PHACOFLEX INSERTER DISPOSABLE CARTRIDGE, AND HANDPIECE, AMO PHACOFLEX INSERTER, FOLDABLE IOL INSERT INSTR
7
Total
7
Cleared
0
Denied
Allergan Medical Optics has 7 FDA 510(k) cleared medical devices. Based in Anasco, US.
Historical record: 7 cleared submissions from 1989 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Allergan Medical Optics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allergan Medical Optics
7 devices
Cleared
Jun 15, 1995
AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM
Ophthalmic
77d
Cleared
Jul 06, 1994
AMO PHACOFLEX INSERTER DISPOSABLE CARTRIDGE, AND HANDPIECE
Ophthalmic
96d
Cleared
Apr 07, 1994
AMO PHACOFLEX INSERTER, FOLDABLE IOL INSERT INSTR
Ophthalmic
440d
Cleared
Jan 07, 1993
AMO(R) FLRX-TIP(TM) DISPOS I/A HANDPIECE, OPO-38
Ophthalmic
80d
Cleared
Dec 23, 1992
AMO ELITE
Ophthalmic
121d
Cleared
Jul 26, 1991
MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM
Ophthalmic
88d
Cleared
Jun 16, 1989
PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR
Ophthalmic
51d