Ocular Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ocular Instruments, Inc. - FDA 510(k) Cleared Devices
50
Total
50
Cleared
0
Denied
Ocular Instruments, Inc. has 50 FDA 510(k) cleared ophthalmic devices. Based in Bellevue, US.
Historical record: 50 cleared submissions from 1984 to 2002.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ocular Instruments, Inc.
50 devices
Cleared
Mar 04, 2002
STAURENGHI WIDE FIELD SCANNING LASER LENS
Ophthalmic
74d
Cleared
Aug 24, 2001
DISPOSABLE VITRECTOMY LENS
Ophthalmic
50d
Cleared
Nov 08, 1994
MANDELKORN SUTURE LYSIS LENS
Ophthalmic
452d
Cleared
Oct 31, 1994
RITCH NYLON SUTURE LASER LENS
Ophthalmic
482d
Cleared
Aug 29, 1994
50 DEGREE HRI PRISM LENS
Ophthalmic
159d
Cleared
Apr 01, 1994
OSHER SURGICAL GONIO/POSTERIOR POLE LENS
Ophthalmic
150d
Cleared
Nov 16, 1992
TROKEL /3 GONIO LASER LENS
Ophthalmic
237d
Cleared
Nov 16, 1992
BYRNE EXPULSIVE LENS
Ophthalmic
117d
Cleared
Dec 09, 1991
PEDIATRIC VITRECTOMY LENS SET
Ophthalmic
90d
Cleared
Nov 13, 1991
LANDERS HIGH REFRACTIVE INDEX VITRECTOMY LENS SET
Ophthalmic
61d
Cleared
Aug 21, 1991
LANDERS WIDE FIELD TEMPORARY KERATOPROSTHESIS
Ophthalmic
175d
Cleared
Aug 07, 1991
LANDERS 3 STRUT IRRIGATING VITRECTOMY LENS RING
Ophthalmic
78d
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