GE Medical Systems Lunar
Country not established
- Devices
- 2
What GE Medical Systems Lunar makes
The company produces software updates and applications for dual-energy X-ray absorptiometry (DXA) bone densitometers, including specialized releases for bone density analysis and body composition assessment. These tools analyze skeletal health and body metrics, such as bone mineral density and fat mass distribution, using DXA technology.
The portfolio consists of Class II medical devices regulated under the FDA’s 510(k) clearance process. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. regulatory requirements. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ge Lunar Body Composition Software Ref K071570
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Medical Systems Lunar have in the registry?
The registry currently lists 2 devices for Ge Medical Systems Lunar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Medical Systems Lunar's devices?
Among its 2 most recently registered devices, Ge Medical Systems Lunar has devices listed in FDA 510(k) (2 devices).
What risk classes do Ge Medical Systems Lunar's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ge Medical Systems Lunar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Medical Systems Lunar in the registry?
The most recently registered devices listed for Ge Medical Systems Lunar include ENCORE 14 SOFTWARE RELEASE FOR THE GE LUNAR DXA BONE DENSITOMETERS and GE LUNAR BODY COMPOSITION SOFTWARE.