Vivus, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Vivus, Inc. makes
Vivus, Inc. manufactures adjustable medical devices for vascular applications, including the ACTIS adjustable constriction loop and the ACTIS venous flow controller. These products are designed to regulate blood flow in specific vascular procedures, such as peripheral interventions.
The company’s portfolio is classified under FDA Class II devices and is authorised through the 510(k) clearance process in the United States. The devices are listed in the FDA’s 510(k) registry, adhering to regulatory requirements for vascular flow control systems.
Catalogue
Actis Adjustable Constriction Loop Ref K003115
510(k) 510(k)Actis (Venous Flow Controller) Ref K962915
510(k) 510(k)
Frequently asked questions
How many devices does Vivus, Inc. have in the registry?
The registry currently lists 2 devices for Vivus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivus, Inc.'s devices?
Among its 2 most recently registered devices, Vivus, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vivus, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vivus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivus, Inc. in the registry?
The most recently registered devices listed for Vivus, Inc. include ACTIS ADJUSTABLE CONSTRICTION LOOP and ACTIS (VENOUS FLOW CONTROLLER).