# American Optisurgical, Inc.

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 6 (1995–2010): 6 510(k) clearances
- Product codes: HQC (5), LFL (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Integra Neurosciences: 1 (https://510kreport.com/company/integra-neurosciences)
- American Optical Corp.: 1 (https://510kreport.com/company/american-optical)
- Surgical Design Corp.: 1 (https://510kreport.com/company/surgical-design)
- Optical Micro Systems, Inc.: 1 (https://510kreport.com/company/optical-micro-systems)

## Firms that cite its devices most
- Tenex Health, Inc.: 1 (https://510kreport.com/company/tenex-health)

## Its most-cited devices
- K101561: TX1 Tissue Removal System (2010), cited by 1
- K020527: Horizon Phacoemulsification System, Model HZN-2030 (2002), cited by 1

## Recent decisions
- K101561: TX1 Tissue Removal System (Aug 27, 2010)
- K080803: Visual Phacoemulsification System, Model 551 (Sep 22, 2008)
- K020527: Horizon Phacoemulsification System, Model HZN-2030 (Jul 9, 2002)
- K953538: RM001 Reusable (Dec 26, 1995)
- K953539: DM001 Disposable Pack (Dec 26, 1995)
- K952331: Aoi LC-40 Phacoemulsifier (Aug 16, 1995)

Source page: https://510kreport.com/company/american-optisurgical