Norland Corp.
United StatesFDA applicant, unverified
- Devices
- 15
What Norland Corp. makes
Norland Corp. manufactures X-ray bone densitometers, including peripheral and whole-body models, for measuring bone mineral density and assessing fracture risk. Their devices include standalone systems like the XCT-900 and XR-26, as well as software options for body composition analysis and reference population data. Additional tools evaluate fracture risk specifically for their bone densitometers, such as the SXA 3000 and Apollo models.
Norland Corp.’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, reflecting their regulatory standing. The company is based in the United States.
Catalogue
Search and filter all 15 devicesFrequently asked questions
How many devices does Norland Corp. have in the registry?
The registry currently lists 15 devices for Norland Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Norland Corp.'s devices?
Among its 15 most recently registered devices, Norland Corp. has devices listed in FDA 510(k) (15 devices).
What risk classes do Norland Corp.'s devices fall under?
Among its 15 most recently registered devices, the classes recorded for Norland Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Norland Corp. in the registry?
The most recently registered devices listed for Norland Corp. include MODEL XCT-900 PQCT X-RAY BONE DENSITOMETER, NORLAND MODEL XR-26 X-RAY BONE DENSITOMETER, LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET and BONE DENSITOMETER.