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FDA 510(k)

Denti.AI Auto-Chart

K-Number: K222054 · 2022-11-22

Decision Date2022-11-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Denti.AI Auto-Chart is a medical device manufactured by Denti.Ai Technology, Inc.. It received FDA 510(k) clearance on 2022-11-22 under approval number K222054. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Denti.AI Auto-Chart?

Denti.AI Auto-Chart is a medical device that received FDA 510(k) clearance on 2022-11-22. It is manufactured by Denti.Ai Technology, Inc.. The 510(k) number is K222054.

When was Denti.AI Auto-Chart approved by the FDA?

Denti.AI Auto-Chart received FDA 510(k) clearance on 2022-11-22, under approval number K222054.

What company makes Denti.AI Auto-Chart?

Denti.AI Auto-Chart is manufactured by Denti.Ai Technology, Inc..

What is the FDA product code for Denti.AI Auto-Chart?

The FDA product code for Denti.AI Auto-Chart is LLZ.

Other Devices by Denti.Ai Technology, Inc.

Related Devices (Code: LLZ)

Official Source

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