Intermedical, Inc.
Country not established
- Devices
- 1
What Intermedical, Inc. makes
Intermedical, Inc. manufactures the IM COLLAGEN SHIELD, a Class I medical device designed for wound protection and skin barrier support.
The IM COLLAGEN SHIELD is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Im Collagen Shield Ref K896449
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intermedical, Inc. have in the registry?
The registry currently lists 1 device for Intermedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intermedical, Inc.'s devices?
Among its 1 most recently registered device, Intermedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intermedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intermedical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intermedical, Inc. in the registry?
The most recently registered devices listed for Intermedical, Inc. include IM COLLAGEN SHIELD.