Vena-Tech, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vena Cava Filter Ref K881604
Regimes: 510(k) Registry: 510(k)Vena Cava Filter Ref K901454
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vena-Tech, Inc. have in the registry?
The registry currently lists 2 devices for Vena-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vena-Tech, Inc.'s devices?
Among its 2 most recently registered devices, Vena-Tech, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vena-Tech, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vena-Tech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vena-Tech, Inc. in the registry?
The most recently registered devices listed for Vena-Tech, Inc. include VENA CAVA FILTER.