Dentalview, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Dentalview, Inc. makes
Dentalview, Inc. manufactures the PerioView System, a diagnostic tool for periodontal assessment, and the PerioView Model DV-1, a fiberscope with a window sheath designed for intraoral imaging of gum tissue.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dentalview Perioview System Ref K973492
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentalview, Inc. have in the registry?
The registry currently lists 2 devices for Dentalview, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentalview, Inc.'s devices?
Among its 2 most recently registered devices, Dentalview, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dentalview, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dentalview, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dentalview, Inc. in the registry?
The most recently registered devices listed for Dentalview, Inc. include DENTALVIEW PERIOVIEW SYSTEM and PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH..