Bausch Health Americas Incorporated
Country not established
- Devices
- 1
What Bausch Health Americas Incorporated makes
Bausch Health Americas Incorporated manufactures BIAFINE Topical Cream, a Class II medical device designed for topical skin applications.
The company’s portfolio is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
BIAFINE Topical Cream Ref K190342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bausch Health Americas Incorporated have in the registry?
The registry currently lists 1 device for Bausch Health Americas Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bausch Health Americas Incorporated's devices?
Among its 1 most recently registered device, Bausch Health Americas Incorporated has devices listed in FDA 510(k) (1 device).
What are the newest devices from Bausch Health Americas Incorporated in the registry?
The most recently registered devices listed for Bausch Health Americas Incorporated include BIAFINE Topical Cream.