# Ophthalmic Technologies, Inc.

- Location (FDA's records): Hasbrouck, NJ
- FDA decisions: 9 (1995–2005): 9 510(k) clearances
- Product codes: IYO (5), HLI (1), FTD (1), HQR (1), MPA (1)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 7 (3 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
- Life Imaging Systems, Inc.: 1 (https://510kreport.com/company/life-imaging-systems)
- Heidelberg Engineering GmbH: 1 (https://510kreport.com/company/heidelberg-engineering)
- Dutch Ophthalmic USA, Inc.: 1 (https://510kreport.com/company/dutch-ophthalmic-usa)
- Ellman Intl., Inc.: 1 (https://510kreport.com/company/ellman-intl)

## Firms that cite its devices most
- Opko Instrumentation, Inc.: 3 (https://510kreport.com/company/opko-instrumentation)
- Opko Health, Inc.: 1 (https://510kreport.com/company/opko-health)

## Its most-cited devices
- K960622: I-SCAN (1996), cited by 3
- K030770: Oti Scan with Transducers (2003), cited by 2
- K031391: HF Module with Transducers (2003), cited by 1
- K042885: Oct-Opthalmoscope (2005), cited by 1

## Recent decisions
- K042885: Oct-Opthalmoscope (Jan 21, 2005)
- K031391: HF Module with Transducers (Jun 20, 2003)
- K030770: Oti Scan with Transducers (Mar 27, 2003)
- K024114: A-SCAN 100 (Jan 10, 2003)
- K990064: DI-Rhex Ophthalmic Diathermy System (Apr 4, 1999)
- K974522: 3D I-Scan (Feb 25, 1998)
- K971679: I-Scope Ophthalmic Endoscope (Jun 25, 1997)
- K960622: I-SCAN (May 13, 1996)

Source page: https://510kreport.com/company/ophthalmic-technologies