# Visijet, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 1 (2000–2000): 1 510(k) clearance
- Product codes: MYD (1)
- Predicates its devices cite: 3 (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
- Barron Precision Instruments, LLC: 1 (https://510kreport.com/company/barron-precision-instruments)
- Medjet, Inc.: 1 (https://510kreport.com/company/medjet)
- Hansa Research & Development, Inc.: 1 (https://510kreport.com/company/hansa-research-development)

## Recent decisions
- K991124: Visijet Hydrokeratome, Model 50 (Oct 20, 2000)

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