Jewell Industries
Country not established
- Devices
- 1
What Jewell Industries makes
Jewell Industries manufactures FABFOAM #302, a foam-based medical device designed for wound care or padding applications, providing cushioning or support in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with FABFOAM #302 listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Fabfoam #302 Ref K894683
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jewell Industries have in the registry?
The registry currently lists 1 device for Jewell Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jewell Industries's devices?
Among its 1 most recently registered device, Jewell Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Jewell Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jewell Industries's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jewell Industries in the registry?
The most recently registered devices listed for Jewell Industries include FABFOAM #302.