Dreve Denatmid GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Dreve Denatmid GmbH makes
Dreve Denatmid GmbH manufactures the Fixtemp® C&B 4:1, a dental device designed for temperature-controlled polymerization of composite resin restorations, ensuring precise curing in clinical settings.
The Fixtemp® C&B 4:1 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Fixtemp® C&B 4:1 Ref K241226
510(k) 510(k)
Frequently asked questions
How many devices does Dreve Denatmid GmbH have in the registry?
The registry currently lists 1 device for Dreve Denatmid GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dreve Denatmid GmbH's devices?
Among its 1 most recently registered device, Dreve Denatmid GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Dreve Denatmid GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dreve Denatmid GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dreve Denatmid GmbH in the registry?
The most recently registered devices listed for Dreve Denatmid GmbH include Fixtemp® C&B 4:1.