Mentor O & O, Inc. is one of 13697 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mentor O & O, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM, MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION, MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM
18
Total
18
Cleared
0
Denied
Mentor O & O, Inc. has 18 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1982 to 1996.
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 - Mentor O & O, Inc.
18 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
May 13, 1991
MENTOR(R) SUR-E-TROL(R)
General Hospital
89d
Cleared
May 02, 1991
MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305
General & Plastic Surgery
48d
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