# Mentor O & O, Inc.

- Location (FDA's records): Norwell, MA
- FDA decisions: 18 (1982–1996): 18 510(k) clearances
- Product codes: HOX (3), HQE (2), HQQ (2), HQC (2), HLI (2), HQR (1), HNR (1), HKP (1), GEI (1), HRM (1), HJG (1), FRN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ion Medical, LLC: 1 (https://510kreport.com/company/ion-medical)

## Its most-cited devices
- K911160: Mentor (R) Wet-Field (R) II AC Coagulator, 22-1305 (1991), cited by 1

## Recent decisions
- K955245: Mentor Meridian Phacoemulsification System (Feb 12, 1996)
- K934320: Mentor Wet-Field Hemostatic Eraser Bipolar Instrument, 20 Gauge with Extrusion Aspiration (Feb 16, 1994)
- K912904: Mentor Odyssey Phacoemulsification System (Jun 11, 1992)
- K915340: Mentor Horizon Low Vision Magnifier (Mar 30, 1992)
- K910637: Mentor (R) Sur-E-Trol (R) (May 13, 1991)
- K911160: Mentor (R) Wet-Field (R) II AC Coagulator, 22-1305 (May 2, 1991)
- K903878: Mentor (R) Durastat (TM) Autoclav Bipolar Hemostat (Nov 5, 1990)
- K895010: Mentor Spectacle Binocular Indirect Ophthalmoscope (Sep 11, 1989)

Source page: https://510kreport.com/company/mentor-o-o