Eagle Vision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eagle Vision, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Eagle Vision, Inc. has 7 FDA 510(k) cleared medical devices. Based in Bethesda, US.
Historical record: 7 cleared submissions from 1988 to 2006. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eagle Vision, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eagle Vision, Inc.
7 devices
Cleared
May 02, 2006
EAGLEVISION GELLANSERTS, MODEL REF 0040
Ophthalmic
152d
Cleared
Apr 25, 2003
MONOCANALICULAR STENTS, LACRIMAL INTUBATION SETS
Ophthalmic
81d
Cleared
Apr 20, 1999
FLEXPLUG
Ophthalmic
18d
Cleared
Jun 06, 1991
EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUG
Ophthalmic
184d
Cleared
May 16, 1989
TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT
Ophthalmic
82d
Cleared
Apr 11, 1989
EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE
Ophthalmic
47d
Cleared
Aug 22, 1988
EV MONOCANALICULAR STENT (TM)
Ophthalmic
21d