3D Imaging Partners, Inc.
Country not established
- Devices
- 1
What 3D Imaging Partners, Inc. makes
3D Imaging Partners, Inc. develops NERVEVISION software systems, which are designed for intraoperative neuronavigation and guidance during surgical procedures.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The company is based in the US.
Catalogue
Nervevision Software Systems Ref K121075
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does 3D Imaging Partners, Inc. have in the registry?
The registry currently lists 1 device for 3D Imaging Partners, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list 3D Imaging Partners, Inc.'s devices?
Among its 1 most recently registered device, 3D Imaging Partners, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do 3D Imaging Partners, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for 3D Imaging Partners, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from 3D Imaging Partners, Inc. in the registry?
The most recently registered devices listed for 3D Imaging Partners, Inc. include NERVEVISION SOFTWARE SYSTEMS.