Mentor O & O, Inc.
Mentor O & O, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1996.
Top product codes for Mentor O & O, Inc.
Recent clearances by Mentor O & O, Inc.
- K955245 — MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM
- K934320 — MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION
- K912904 — MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEM
- K915340 — MENTOR HORIZON LOW VISION MAGNIFIER
- K910637 — MENTOR(R) SUR-E-TROL(R)
- K911160 — MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305
- K903878 — MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT
- K895010 — MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPE
- K890622 — SURG-E-TROL SYSTEM I AND SYSTEM II
- K890595 — MENTOR ANTERIOR SEGMENT VITRECTOR
- K881001 — MENTOR WET-FIELD*II COAGULATOR
- K875112 — MENTOR B-VAT(TM) II VIDEO TESTER
- K853736 — MENTOR BRIGHTNESS ACUITY TESTER
- K853382 — MAID MENTOR ASPIRATION/IRRIGATION DEVRO
- K850270 — CORNEAL LIGHT SHIELD
- K843304 — BINOCULAR INDIRECT OPHTHALMOSCOPE
- K844129 — SHURE GRIP TYING FORCEPS
- K821932 — MENTOR POTENTIAL ACUITY METER
Data sourced from openFDA. This site is unofficial and independent of the FDA.