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Ocular Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
50
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K014170STAURENGHI WIDE FIELD SCANNING LASER LENSMarch 4, 2002
K012096DISPOSABLE VITRECTOMY LENSAugust 24, 2001
K933976MANDELKORN SUTURE LYSIS LENSNovember 8, 1994
K933264RITCH NYLON SUTURE LASER LENSOctober 31, 1994
K94142050 DEGREE HRI PRISM LENSAugust 29, 1994
K935302OSHER SURGICAL GONIO/POSTERIOR POLE LENSApril 1, 1994
K923670BYRNE EXPULSIVE LENSNovember 16, 1992
K921414TROKEL /3 GONIO LASER LENSNovember 16, 1992
K914051PEDIATRIC VITRECTOMY LENS SETDecember 9, 1991
K914117LANDERS HIGH REFRACTIVE INDEX VITRECTOMY LENS SETNovember 13, 1991
K910828LANDERS WIDE FIELD TEMPORARY KERATOPROSTHESISAugust 21, 1991
K912253LANDERS 3 STRUT IRRIGATING VITRECTOMY LENS RINGAugust 7, 1991
K912269LANDERS NOTCHED IRRIGATING VITRECTOMY LENS RINGAugust 7, 1991
K912268LANDERS NOTCHED VITRECTOMY LENS RINGAugust 7, 1991
K912151LANDERS THREE STRUT VITRECTOMY LENS RINGJuly 25, 1991
K912366MAINSTER HIGH MAGNIFICATION LASER LENSJune 25, 1991
K910231NMR-K FUNDUS LASER LENSJanuary 28, 1991
K902496LANDERS VITRECTOMY LENS RING W/INFUSIONJuly 24, 1990
K895846TWO MIRROR GONIO LENSDecember 18, 1989
K896198MAINSTER WIDE FIELD LASER LENSDecember 18, 1989