Curapharm, Inc.
Country not established
- Devices
- 1
What Curapharm, Inc. makes
Curapharm, Inc. produces modifications to Phytacare Alginate Hydrogel Wound Filler, a product designed for wound care applications.
The company’s portfolio is regulated under FDA Class II (U) devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Curapharm, Inc. have in the registry?
The registry currently lists 1 device for Curapharm, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curapharm, Inc.'s devices?
Among its 1 most recently registered device, Curapharm, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Curapharm, Inc. in the registry?
The most recently registered devices listed for Curapharm, Inc. include MODIFICATION TO PHYTACARE ALGINATE HYDROGEL WOUND FILLER.