Stiefel Laboratories, Inc.
Country not established
- Devices
- 1
What Stiefel Laboratories, Inc. makes
Stiefel Laboratories, Inc. manufactures Impruv A.I. Cream, a wound and skin emulsion designed for topical application to promote healing and skin repair.
The product is classified as Class II (U) under FDA regulations and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Impruv A.I. Cream Wound And Skin Emulsion Ref K041342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stiefel Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Stiefel Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stiefel Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Stiefel Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Stiefel Laboratories, Inc. in the registry?
The most recently registered devices listed for Stiefel Laboratories, Inc. include IMPRUV A.I. CREAM WOUND AND SKIN EMULSION.