Miele, Inc.
Country not established
- Devices
- 1
What Miele, Inc. makes
Miele, Inc. manufactures dental thermal disinfectors, such as the Model G7881, designed for sterilizing dental instruments and reusable equipment using heat-based processes.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Miele Dental Thermal Disinfector, Model G7881 Ref K031799
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Miele, Inc. have in the registry?
The registry currently lists 1 device for Miele, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Miele, Inc.'s devices?
Among its 1 most recently registered device, Miele, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Miele, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Miele, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Miele, Inc. in the registry?
The most recently registered devices listed for Miele, Inc. include MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881.