# Visionex, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 2 (1988–1991): 2 510(k) clearances
- Product codes: KYF (1), KYD (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K902296: Trabeculo-Suprachoroidal Shunt (Mar 14, 1991)
- K881515: Tear Volume Tests (May 23, 1988)

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