Mentor O & O, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K955245MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEMFebruary 12, 1996
K934320MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATIONFebruary 16, 1994
K912904MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEMJune 11, 1992
K915340MENTOR HORIZON LOW VISION MAGNIFIERMarch 30, 1992
K910637MENTOR(R) SUR-E-TROL(R)May 13, 1991
K911160MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305May 2, 1991
K903878MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTATNovember 5, 1990
K895010MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPESeptember 11, 1989
K890622SURG-E-TROL SYSTEM I AND SYSTEM IIMay 4, 1989
K890595MENTOR ANTERIOR SEGMENT VITRECTORApril 17, 1989
K881001MENTOR WET-FIELD*II COAGULATORMay 13, 1988
K875112MENTOR B-VAT(TM) II VIDEO TESTERMarch 8, 1988
K853736MENTOR BRIGHTNESS ACUITY TESTERNovember 1, 1985
K853382MAID MENTOR ASPIRATION/IRRIGATION DEVROOctober 4, 1985
K850270CORNEAL LIGHT SHIELDMay 31, 1985
K843304BINOCULAR INDIRECT OPHTHALMOSCOPENovember 21, 1984
K844129SHURE GRIP TYING FORCEPSNovember 21, 1984
K821932MENTOR POTENTIAL ACUITY METERAugust 3, 1982