# Transphoton Corporation

- Location (FDA's records): Lunenburg, MA
- FDA decisions: 2 (2003–2007): 2 510(k) clearances
- Product codes: KPS (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 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
- Nuclear Cardiology Systems, Inc.: 1 (https://510kreport.com/company/nuclear-cardiology-systems)
- Ge Medical Systems F.I. Haifa: 1 (https://510kreport.com/company/ge-medical-systems-fi-haifa)
- Cardiarc, Ltd.: 1 (https://510kreport.com/company/cardiarc)

## Its most-cited devices
- K033001: Apex Detector Electronics & Acquisition Interface, Model XL-4 (2003), cited by 1

## Recent decisions
- K070589: C! (Apr 24, 2007)
- K033001: Apex Detector Electronics & Acquisition Interface, Model XL-4 (Dec 24, 2003)

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