Fouts Development, Inc.
Country not established
- Devices
- 1
What Fouts Development, Inc. makes
Fouts Development, Inc. manufactures the TWIXEL™, a medical device designed for [specific application not detailed in data]. The product is intended for [intended use not detailed in data], adhering to [functional purpose not detailed in data] standards.
The TWIXEL™ falls under Class I regulatory classification in the U.S. and is listed under the FDA 510(k) pathway. The company operates from the United States.
Catalogue
Twixel(Tm) Ref K885056
510(k) 510(k)
Frequently asked questions
How many devices does Fouts Development, Inc. have in the registry?
The registry currently lists 1 device for Fouts Development, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fouts Development, Inc.'s devices?
Among its 1 most recently registered device, Fouts Development, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fouts Development, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fouts Development, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fouts Development, Inc. in the registry?
The most recently registered devices listed for Fouts Development, Inc. include TWIXEL(TM).