Denti.Ai Technology, Inc.
CanadaFDA 510(k) applicant, unverified FDA
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Denti.Ai Technology, Inc. makes
Denti.Ai Technology, Inc. develops dental software devices, including Denti.AI Auto-Chart and Denti.AI Detect, which are designed to assist with dental charting and detection processes.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Denti.Ai Technology, Inc. is based in the US.
Catalogue
- GUDID
- GUDID
Denti.AI Auto-Chart Ref K222054
510(k) 510(k)Denti.AI Detect Ref K230144
510(k) 510(k)
Company details
- DUNS number
- 204120372
FDA establishments
- Denti.ai Technology Inc. Toronto Ontario · CA FEI 3029956998
Frequently asked questions
How many devices does Denti.Ai Technology, Inc. have in the registry?
The registry currently lists 4 devices for Denti.Ai Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Denti.Ai Technology, Inc.'s devices?
Among its 4 most recently registered devices, Denti.Ai Technology, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Denti.Ai Technology, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Denti.Ai Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Denti.Ai Technology, Inc. in the registry?
The most recently registered devices listed for Denti.Ai Technology, Inc. include Denti.AI Auto-Chart 21.06.22, Denti.AI Detect 1.3, Denti.AI Auto-Chart and Denti.AI Detect.
Which FDA establishments are linked to Denti.Ai Technology, Inc.?
1 FDA establishment is linked to Denti.Ai Technology, Inc. in the registry; they are listed on the company page.