Denti.AI Detect— 510(k) K230144
Substantially EquivalentDenti.Ai Technology, Inc.
FDA 510(k) clearance K230144 for Denti.AI Detect, Substantially Equivalent on 2023-10-06. Applicant: Denti.Ai Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Denti.Ai Technology, Inc.
- Product code
- Code MYN
- Device class
- Class 2
- Regulation
- 21 CFR 892.2070
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, CA
Recent devices under product code MYN
view allMore clearances from Denti.Ai Technology, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.