Alcon Lensx, Inc. is one of 5363 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alcon Lensx, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Alcon Lensx, Inc. has 2 FDA 510(k) cleared medical devices. Based in Laguna Beach, US.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Alcon Lensx, Inc. Filter by specialty or product code using the sidebar.
Alcon Lensx, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 12, 2012
LENSX LASER SYSTEM
Ophthalmic
70d
Cleared
Sep 06, 2012
LENSSX LASER SYSTEM
Ophthalmic
181d