Ideamatrix
Country not established
- Devices
- 2
What Ideamatrix makes
Ideamatrix manufactures needle sets designed for medical procedures, including the TRU-CORE and ECHO STAR models. These devices are intended for precise and controlled injections or aspirations, supporting clinical applications in various specialties.
The company’s needle sets are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. They are based in the United States.
Catalogue
Tru-Core Needle Set Ref K943368
Regimes: 510(k) Registry: 510(k)Echo Star Needle Set Ref K945921
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ideamatrix have in the registry?
The registry currently lists 2 devices for Ideamatrix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ideamatrix's devices?
Among its 2 most recently registered devices, Ideamatrix has devices listed in FDA 510(k) (2 devices).
What risk classes do Ideamatrix's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ideamatrix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ideamatrix in the registry?
The most recently registered devices listed for Ideamatrix include TRU-CORE NEEDLE SET and ECHO STAR NEEDLE SET.