Inpharma
Country not established
- Devices
- 1
What Inpharma makes
Inpharma manufactures DURAPHAT, a dental adhesive used to bond restorative materials to tooth surfaces, ensuring durable and long-lasting dental repairs.
The company’s portfolio is regulated under FDA Class II devices, with DURAPHAT authorised via 510(k) clearance. The product is listed in the FDA’s 510(k) database. Inpharma operates from the United States.
Catalogue
Duraphat Ref K945794
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inpharma have in the registry?
The registry currently lists 1 device for Inpharma. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inpharma's devices?
Among its 1 most recently registered device, Inpharma has devices listed in FDA 510(k) (1 device).
What risk classes do Inpharma's devices fall under?
Among its 1 most recently registered device, the classes recorded for Inpharma's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inpharma in the registry?
The most recently registered devices listed for Inpharma include DURAPHAT.