Integration Diagnostics, Ltd.
Country not established
- Devices
- 2
What Integration Diagnostics, Ltd. makes
Integration Diagnostics, Ltd. manufactures diagnostic devices for bone quality assessment, including the OSSTELL Resonance Frequency Analyzer, which measures bone stiffness, and the OSSTELL Mentor RFA, a handheld device for resonance frequency analysis.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Osstell Resonance Frequency Analyzer Ref K003714
Regimes: 510(k) Registry: 510(k)Osstell Mentor Rfa Ref K033689
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integration Diagnostics, Ltd. have in the registry?
The registry currently lists 2 devices for Integration Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integration Diagnostics, Ltd.'s devices?
Among its 2 most recently registered devices, Integration Diagnostics, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Integration Diagnostics, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Integration Diagnostics, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Integration Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Integration Diagnostics, Ltd. include OSSTELL RESONANCE FREQUENCY ANALYZER and OSSTELL MENTOR RFA.