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FDA 510(k)

Videa Dental AI

K-Number: K251002 · 2025-09-19

ApplicantVideahealth, Inc.
Decision Date2025-09-19
Product CodeMYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Videa Dental AI is a medical device manufactured by Videahealth, Inc.. It received FDA 510(k) clearance on 2025-09-19 under approval number K251002. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Videa Dental AI?

Videa Dental AI is a medical device that received FDA 510(k) clearance on 2025-09-19. It is manufactured by Videahealth, Inc.. The 510(k) number is K251002.

When was Videa Dental AI approved by the FDA?

Videa Dental AI received FDA 510(k) clearance on 2025-09-19, under approval number K251002.

What company makes Videa Dental AI?

Videa Dental AI is manufactured by Videahealth, Inc..

What is the FDA product code for Videa Dental AI?

The FDA product code for Videa Dental AI is MYN.

Other Devices by Videahealth, Inc.

K213795Videa Caries Assist K232384Videa Dental Assist K223296Videa Perio Assist

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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