Alpha Intelligence Manifolds, Inc.
TaiwanFDA applicant, unverified
- Devices
- 2
What Alpha Intelligence Manifolds, Inc. makes
Alpha Intelligence Manifolds, Inc. manufactures the DeepXray, a medical imaging device designed for advanced radiographic analysis.
The DeepXray is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
DeepXray Spina Ref K253192
Regimes: 510(k) Registry: 510(k)DeepXray Ref K223621
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alpha Intelligence Manifolds, Inc. have in the registry?
The registry currently lists 2 devices for Alpha Intelligence Manifolds, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alpha Intelligence Manifolds, Inc.'s devices?
Among its 2 most recently registered devices, Alpha Intelligence Manifolds, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alpha Intelligence Manifolds, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alpha Intelligence Manifolds, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alpha Intelligence Manifolds, Inc. in the registry?
The most recently registered devices listed for Alpha Intelligence Manifolds, Inc. include DeepXray Spina and DeepXray.