# Kgt, Inc.

- Location (FDA's records): Austin, TX
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: JAK (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Vida Diagnostics, Inc.: 1 (https://510kreport.com/company/vida-diagnostics)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)
- Superdimension, Ltd.: 1 (https://510kreport.com/company/superdimension)

## Firms that cite its devices most
- Cybernet Systems Co., Ltd.: 1 (https://510kreport.com/company/cybernet-systems)

## Its most-cited devices
- K093810: BF-Navi (2010), cited by 1

## Recent decisions
- K093810: BF-Navi (Jun 18, 2010)

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