American Optisurgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Optisurgical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
American Optisurgical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 6 cleared submissions from 1995 to 2010. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by American Optisurgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Optisurgical, Inc.
6 devices
Cleared
Aug 27, 2010
TX1 TISSUE REMOVAL SYSTEM
General & Plastic Surgery
84d
Cleared
Sep 22, 2008
VISUAL PHACOEMULSIFICATION SYSTEM, MODEL 551
Ophthalmic
185d
Cleared
Jul 09, 2002
HORIZON PHACOEMULSIFICATION SYSTEM, MODEL HZN-2030
Ophthalmic
140d
Cleared
Dec 26, 1995
RM001 REUSABLE
Ophthalmic
151d
Cleared
Dec 26, 1995
DM001 DISPOSABLE PACK
Ophthalmic
151d
Cleared
Aug 16, 1995
AOI LC-40 PHACOEMULSIFIER
Ophthalmic
90d