Mentor O & O, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mentor O & O, Inc. Ophthalmic ✕
15 devices
Cleared
Feb 12, 1996
MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM
Ophthalmic
89d
Cleared
Feb 16, 1994
MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH...
Ophthalmic
166d
Cleared
Jun 11, 1992
MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM
Ophthalmic
345d
Cleared
Mar 30, 1992
MENTOR HORIZON LOW VISION MAGNIFIER
Ophthalmic
158d
Cleared
Nov 05, 1990
MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT
Ophthalmic
75d
Cleared
Sep 11, 1989
MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPE
Ophthalmic
34d
Cleared
May 04, 1989
SURG-E-TROL SYSTEM I AND SYSTEM II
Ophthalmic
86d
Cleared
Apr 17, 1989
MENTOR ANTERIOR SEGMENT VITRECTOR
Ophthalmic
70d
Cleared
May 13, 1988
MENTOR WET-FIELD*II COAGULATOR
Ophthalmic
65d
Cleared
Mar 08, 1988
MENTOR B-VAT(TM) II VIDEO TESTER
Ophthalmic
84d
Cleared
Nov 01, 1985
MENTOR BRIGHTNESS ACUITY TESTER
Ophthalmic
56d
Cleared
Oct 04, 1985
MAID MENTOR ASPIRATION/IRRIGATION DEVRO
Ophthalmic
53d