Martz, Inc.
Country not established
- Devices
- 1
What Martz, Inc. makes
Martz, Inc. manufactures the Dentti System, a dental device designed for intraoral imaging and diagnostic procedures.
The Dentti System is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dentti System Ref K151965
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martz, Inc. have in the registry?
The registry currently lists 1 device for Martz, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martz, Inc.'s devices?
Among its 1 most recently registered device, Martz, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Martz, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Martz, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Martz, Inc. in the registry?
The most recently registered devices listed for Martz, Inc. include Dentti System.