Adpharma, Inc.
Country not established
- Devices
- 1
What Adpharma, Inc. makes
Adpharma, Inc. manufactures dentin tubule agents, including the Occlude and Occlude F formulations, designed to seal dentin tubules in dental procedures.
These products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adpharma, Inc. have in the registry?
The registry currently lists 1 device for Adpharma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adpharma, Inc.'s devices?
Among its 1 most recently registered device, Adpharma, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Adpharma, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Adpharma, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adpharma, Inc. in the registry?
The most recently registered devices listed for Adpharma, Inc. include ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT.