# Topex, Inc.

- Location (FDA's records): Danbury, CT
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: JAD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Pantak, Inc.: 1 (https://510kreport.com/company/pantak)
- Gulmay Medical, Ltd.: 1 (https://510kreport.com/company/gulmay-medical)

## Firms that cite its devices most
- Nucletron Corp.: 1 (https://510kreport.com/company/nucletron)
- Sensus Healthcare, Inc.: 1 (https://510kreport.com/company/sensus-healthcare)

## Its most-cited devices
- K063456: SRT100 Superficial Radiation Therapy System (2007), cited by 2

## Recent decisions
- K063456: SRT100 Superficial Radiation Therapy System (Jan 9, 2007)

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