C.V.I., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What C.V.I., Inc. makes
C.V.I., Inc. manufactures surgical instruments and the MEDAID device, a medical aid tool designed for procedural support.
The company’s portfolio includes Class I and Class II devices, all of which are subject to FDA 510(k) clearance requirements. These products are listed under the U.S. regulatory framework and are based in the United States.
Catalogue
Surgical Instruments Ref K811686
510(k) 510(k)Medaid Ref K810841
510(k) 510(k)
Frequently asked questions
How many devices does C.V.I., Inc. have in the registry?
The registry currently lists 2 devices for C.V.I., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.V.I., Inc.'s devices?
Among its 2 most recently registered devices, C.V.I., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do C.V.I., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for C.V.I., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from C.V.I., Inc. in the registry?
The most recently registered devices listed for C.V.I., Inc. include SURGICAL INSTRUMENTS and MEDAID.