# Surgistar, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 4 (1992–2003): 4 510(k) clearances
- Product codes: HNO (2), GDX (1), GCJ (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (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
- Moria SA: 2 (https://510kreport.com/company/moria)
- Chiron Vision Corp.: 1 (https://510kreport.com/company/chiron-vision)
- Plancon Instruments: 1 (https://510kreport.com/company/plancon-instruments)

## Recent decisions
- K030891: Surgistar Microkeratome Blade, Model NO. 2400-LSK (Jun 17, 2003)
- K992978: Ricrokeratome Blade (Nov 16, 1999)
- K941747: Surgistar Trocars (Jul 1, 1994)
- K923689: Surgistar Blades (Sep 9, 1992)

Source page: https://510kreport.com/company/surgistar