Cambridgemed
Country not established
- Devices
- 1
What Cambridgemed makes
Cambridgemed manufactures CLEARADEX GEL, a medical device designed for wound care and debridement, intended to facilitate the removal of necrotic tissue and promote healing in chronic or acute wounds.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices, and its products are listed in the U.S. regulatory database. The manufacturer operates from the United States.
Catalogue
Clearadex Gel Ref K060561
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cambridgemed have in the registry?
The registry currently lists 1 device for Cambridgemed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cambridgemed's devices?
Among its 1 most recently registered device, Cambridgemed has devices listed in FDA 510(k) (1 device).
What risk classes do Cambridgemed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cambridgemed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cambridgemed in the registry?
The most recently registered devices listed for Cambridgemed include CLEARADEX GEL.