The Varner Group, Inc.
Country not established
- Devices
- 1
What The Varner Group, Inc. makes
The Varner Group, Inc. manufactures the TRACHE-TITE, a device designed for securing tracheostomy tubes in place to prevent displacement or accidental removal.
The TRACHE-TITE is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Trache-Tite Ref K950930
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Varner Group, Inc. have in the registry?
The registry currently lists 1 device for The Varner Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Varner Group, Inc.'s devices?
Among its 1 most recently registered device, The Varner Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The Varner Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Varner Group, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Varner Group, Inc. in the registry?
The most recently registered devices listed for The Varner Group, Inc. include TRACHE-TITE.