Aibolit Technologies, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Aibolit Technologies, LLC makes
Aibolit Technologies, LLC manufactures the AIBOLIT 3D+, a medical imaging device designed for three-dimensional visualization and diagnostic applications in clinical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Aibolit 3D+ Ref K211443
Regimes: 510(k) Registry: 510(k)Aibolit 3D+ Ref K222458
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aibolit Technologies, LLC have in the registry?
The registry currently lists 2 devices for Aibolit Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aibolit Technologies, LLC's devices?
Among its 2 most recently registered devices, Aibolit Technologies, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Aibolit Technologies, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aibolit Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aibolit Technologies, LLC in the registry?
The most recently registered devices listed for Aibolit Technologies, LLC include AIBOLIT 3D+.