# Lorad Medical Systems, Inc.

- Location (FDA's records): Danbury, CT
- FDA decisions: 8 (1984–1992): 8 510(k) clearances
- Product codes: IZH (5), JAC (1), EHD (1), IZL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Philips Medical Systems North America, Inc.: 1 (https://510kreport.com/company/philips-medical-systems-north-america)
- Trex Medical Corp.: 1 (https://510kreport.com/company/trex-medical)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)

## Its most-cited devices
- K894643: RT-125 Rough Terrain Mobile X-Ray Unit (1989), cited by 2
- K921962: Lorad Digital Spot Mammography (1992), cited by 1

## Recent decisions
- K921962: Lorad Digital Spot Mammography (Nov 23, 1992)
- K922619: Digitizer, Model # 3-000A-1518 (Jul 1, 1992)
- K913732: Mammographic X-Ray System (Feb 3, 1992)
- K913478: Radiographic Film Marking System (Oct 15, 1991)
- K894935: S-70 Portable Dental X-Ray System (Apr 25, 1990)
- K894643: RT-125 Rough Terrain Mobile X-Ray Unit (Dec 14, 1989)
- K882875: Stereotactic Breast Lesion Localization Accessory (Nov 7, 1988)
- K842102: LORAD (Jul 17, 1984)

Source page: https://510kreport.com/company/lorad-medical-systems