# Exergen Corp.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: FLL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 17 (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 that cite its devices most
- Medisim, Ltd.: 2 (https://510kreport.com/company/medisim)
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Tecnimed S.R.L.: 1 (https://510kreport.com/company/tecnimed)
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-mindray-bio-medical-electronics)
- Schiller AG: 1 (https://510kreport.com/company/schiller)
- Midmark Corp.: 1 (https://510kreport.com/company/midmark)
- Valeo Corp.: 1 (https://510kreport.com/company/valeo)

## Its most-cited devices
- K011291: Temporalscanner Thermometer, Sensortouch (2001), cited by 17

## Recent decisions
- K011291: Temporalscanner Thermometer, Sensortouch (Jul 12, 2001)

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