Indevus Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Indevus Pharmaceuticals, Inc. makes
Indevus Pharmaceuticals, Inc. makes the GK-101E caries removal agent/system, a device designed for the removal of dental caries.
The GK-101E is classified as a Class III medical device and is listed in the FDA Premarket Approval (PMA) database; the company is based in the United States.
Catalogue
Gk-101E Caries Removal Agent/System Ref P830035
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Indevus Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Indevus Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Indevus Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Indevus Pharmaceuticals, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Indevus Pharmaceuticals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Indevus Pharmaceuticals, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Indevus Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Indevus Pharmaceuticals, Inc. include GK-101E CARIES REMOVAL AGENT/SYSTEM.