Avicena, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Avicena, LLC makes
Avicena, LLC manufactures the Vivio® LVEDP System, a device for measuring left ventricular end-diastolic pressure (LVEDP) in cardiac patients, and the Vivio System, a related monitoring solution for hemodynamic assessment.
The company’s portfolio is regulated under Class II devices in the U.S. and includes products listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Vivio® LVEDP System Ref K223905
510(k) 510(k)Vivio System Ref K183710
510(k) 510(k)
Frequently asked questions
How many devices does Avicena, LLC have in the registry?
The registry currently lists 2 devices for Avicena, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avicena, LLC's devices?
Among its 2 most recently registered devices, Avicena, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Avicena, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Avicena, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avicena, LLC in the registry?
The most recently registered devices listed for Avicena, LLC include Vivio® LVEDP System and Vivio System.