K251002
- 510(k) number
- K251002
- Device name
- Videa Dental AI
- Applicant
- Videahealth, Inc. MA · US
- Product code
- MYN — Analyzer, Medical Image
- Decision date
- 2025-09-19
- Date received
- 2025-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K251002.pdf
Official FDA record: K251002
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.