# Gammex, Inc.

- Location (FDA's records): Middleton, WI
- FDA decisions: 3 (1995–2015): 3 510(k) clearances
- Product codes: LMD (1), IYE (1), IWE (1)
- Predicates its devices cite: 3 (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

## Firms whose devices it cites most
- Victoreen, Inc.: 1 (https://510kreport.com/company/victoreen)
- Philips Medical Systems North America, Inc.: 1 (https://510kreport.com/company/philips-medical-systems-north-america)
- Diacor, Inc.: 1 (https://510kreport.com/company/diacor)

## Recent decisions
- K152303: CT Sim Laser System (Sep 11, 2015)
- K954564: Pid-1 Precision Intelligent Dosimeter (Apr 22, 1996)
- K953514: Courier II (Oct 7, 1995)

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