# Mentor Ophthalmics, Inc.

- Location (FDA's records): Norwell, MA
- FDA decisions: 4 (1996–1997): 4 510(k) clearances
- Product codes: HKY (1), KKX (1), HQO (1), IYO (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Teknar, Inc.: 1 (https://510kreport.com/company/teknar)

## Firms that cite its devices most
- Accutome, Inc.: 1 (https://510kreport.com/company/accutome)
- Accutome Ultrasound, Inc.: 1 (https://510kreport.com/company/accutome-ultrasound)
- Neomedix Corp.: 1 (https://510kreport.com/company/neomedix)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)

## Its most-cited devices
- K960765: Mentor Advent a/B System (1996), cited by 2
- K964312: Mentor Tono-Pen 3 (1996), cited by 1
- K971538: Mentor Gemini Hemostatic Eraser (1997), cited by 1

## Recent decisions
- K973146: Mentor Super Absorbent Drape (Dec 4, 1997)
- K971538: Mentor Gemini Hemostatic Eraser (Jul 14, 1997)
- K964312: Mentor Tono-Pen 3 (Nov 26, 1996)
- K960765: Mentor Advent a/B System (Aug 8, 1996)

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