# Ge Lunar Corp.

- Location (FDA's records): Madison, WI
- FDA decisions: 4 (1998–2003): 3 510(k) clearances and 1 original PMA approval
- Product codes: KGI (3), MUA (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 10 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lunar Corp.: 6 (https://510kreport.com/company/lunar)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)

## Firms that cite its devices most
- Ge Medical Systems Ultrasound and Primary Care Dia: 5 (https://510kreport.com/company/ge-medical-systems-ultrasound-and-primary-care-dia)
- Ge Medical Systems China Co., Ltd.: 1 (https://510kreport.com/company/ge-medical-systems-china)
- O.N. Diagnostics: 1 (https://510kreport.com/company/on-diagnostics)
- GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC: 1 (https://510kreport.com/company/ge-medical-systems-ultrasound-primary-care-diagnostics)
- Optasia Medical: 1 (https://510kreport.com/company/optasia-medical)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)

## Its most-cited devices
- K011917: Advanced Hip Assessment Software (2001), cited by 5
- K023554: Dual-Energy Vertebral Assessment View Software (2002), cited by 4
- P970040: Achilles Express Ultrasonometer (1998), cited by 1

## Recent decisions
- K030962: DPX Series Bravo Duo Bone Densitometer (Jul 25, 2003)
- K023554: Dual-Energy Vertebral Assessment View Software (Dec 20, 2002)
- K011917: Advanced Hip Assessment Software (Aug 3, 2001)
- P970040: Achilles Express Ultrasonometer (Jun 26, 1998)

Source page: https://510kreport.com/company/ge-lunar