Foam Tek, Inc.
Country not established
- Devices
- 1
What Foam Tek, Inc. makes
Foam Tek, Inc. manufactures the CONTEX, a Class I medical device designed for foam-based applications in wound care or surface cleaning.
The CONTEX is regulated under the FDA’s 510(k) pathway and is listed in the U.S. as a Class I device. The company is based in the United States.
Catalogue
Contex Ref K790995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Foam Tek, Inc. have in the registry?
The registry currently lists 1 device for Foam Tek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Foam Tek, Inc.'s devices?
Among its 1 most recently registered device, Foam Tek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Foam Tek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Foam Tek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Foam Tek, Inc. in the registry?
The most recently registered devices listed for Foam Tek, Inc. include CONTEX.